ENST00000346798.8:c.2211+1G>T
MANE Select

ENSP00000284981.4:p.=


ENST00000346798.7:c.2211+1G>T

ENSP00000284981.4:p.=


ENST00000348990.9:c.1986+1G>T

ENSP00000345463.5:p.=


ENST00000354192.7:c.1818+1G>T

ENSP00000346129.3:p.=


ENST00000357903.7:c.2154+1G>T

ENSP00000350578.3:p.=


ENST00000358918.7:c.2157+1G>T

ENSP00000351796.3:p.=


ENST00000359726.7:c.1881+1G>T

ENSP00000352760.4:p.=


ENST00000439274.6:c.2043+1G>T

ENSP00000398879.2:p.=


ENST00000440126.7:c.2139+1G>T

ENSP00000387483.2:p.=


ENST00000464867.1:n.558+1G>T



NM_000484.3:c.2211+1G>T

NP_000475.1:p.=


NM_001136016.3:c.2139+1G>T

NP_001129488.1:p.=


NM_001136129.2:c.1818+1G>T

NP_001129601.1:p.=


NM_001136130.2:c.2043+1G>T

NP_001129602.1:p.=


NM_001136131.2:c.1881+1G>T

NP_001129603.1:p.=


NM_001204301.1:c.2157+1G>T

NP_001191230.1:p.=


NM_001204302.1:c.2100+1G>T

NP_001191231.1:p.=


NM_001204303.1:c.1932+1G>T

NP_001191232.1:p.=


NM_201413.2:c.2154+1G>T

NP_958816.1:p.=


NM_201414.2:c.1986+1G>T

NP_958817.1:p.=


NM_000484.4:c.2211+1G>T
MANE Select

NP_000475.1:p.=


NM_001136129.3:c.1818+1G>T

NP_001129601.1:p.=


NM_001136130.3:c.2043+1G>T

NP_001129602.1:p.=


NM_001204301.2:c.2157+1G>T

NP_001191230.1:p.=


NM_001204302.2:c.2100+1G>T

NP_001191231.1:p.=


NM_001204303.2:c.1932+1G>T

NP_001191232.1:p.=


NM_201413.3:c.2154+1G>T

NP_958816.1:p.=


NM_201414.3:c.1986+1G>T

NP_958817.1:p.=


NM_001136131.3:c.1881+1G>T

NP_001129603.1:p.=


NM_001385253.1:c.2043+1G>T

NP_001372182.1:p.=

