ENST00000592092.2:n.422T>G
|
|
|
ENST00000673918.2:c.6050T>G
|
ENSP00000501283.1:p.Val2017Gly
|
|
ENST00000674114.2:c.3657T>G
|
ENSP00000501039.2:n.3657T>G
|
|
ENST00000684977.1:c.1334T>G
|
ENSP00000509384.1:p.Val445Gly
|
|
ENST00000689544.1:n.1269T>G
|
|
|
ENST00000691421.1:c.1337T>G
|
ENSP00000508674.1:p.Val446Gly
|
|
ENST00000691855.1:c.5658T>G
|
|
|
ENST00000692961.1:c.6116T>G
|
ENSP00000509289.1:p.Val2039Gly
|
|
ENST00000693677.1:c.704+336T>G
|
ENSP00000509779.1:n.704+336T>G
|
|
ENST00000420124.4:c.6116T>G
MANE Select
|
ENSP00000398837.2:p.Val2039Gly
|
|
ENST00000673918.1:c.6050T>G
|
ENSP00000501283.1:p.Val2017Gly
|
|
ENST00000674114.1:c.3438T>G
|
|
|
ENST00000420124.2:c.6116T>G
|
ENSP00000398837.1:p.Val2039Gly
|
|
NM_014727.2:c.6116T>G
|
NP_055542.1:p.Val2039Gly
|
|
XM_011527561.1:c.6050T>G
|
XP_011525863.1:p.Val2017Gly
|
|
XM_011527562.1:c.6116T>G
|
XP_011525864.1:p.Val2039Gly
|
|
XM_011527563.1:c.5840T>G
|
XP_011525865.1:p.Val1947Gly
|
|
XM_011527561.2:c.5552T>G
|
XP_011525863.2:p.Val1851Gly
|
|
XM_011527562.2:c.6116T>G
|
XP_011525864.1:p.Val2039Gly
|
|
XM_017027544.1:c.6116T>G
|
XP_016883033.1:p.Val2039Gly
|
|
XM_017027545.1:c.5552T>G
|
XP_016883034.1:p.Val1851Gly
|
|
XM_017027546.1:c.3080T>G
|
XP_016883035.1:p.Val1027Gly
|
|
NM_014727.3:c.6116T>G
MANE Select
|
NP_055542.1:p.Val2039Gly
|
|