ENST00000592092.2:n.701G>C
|
|
|
ENST00000673918.2:c.6329G>C
|
ENSP00000501283.1:p.Arg2110Thr
|
|
ENST00000674114.2:c.3936G>C
|
ENSP00000501039.2:n.3936G>C
|
|
ENST00000684977.1:c.1613G>C
|
ENSP00000509384.1:p.Arg538Thr
|
|
ENST00000689544.1:n.1548G>C
|
|
|
ENST00000691421.1:c.1616G>C
|
ENSP00000508674.1:p.Arg539Thr
|
|
ENST00000691855.1:c.5937G>C
|
|
|
ENST00000692961.1:c.6395G>C
|
ENSP00000509289.1:p.Arg2132Thr
|
|
ENST00000693677.1:c.704+615G>C
|
ENSP00000509779.1:n.704+615G>C
|
|
ENST00000420124.4:c.6395G>C
MANE Select
|
ENSP00000398837.2:p.Arg2132Thr
|
|
ENST00000673918.1:c.6329G>C
|
ENSP00000501283.1:p.Arg2110Thr
|
|
ENST00000674114.1:c.3717G>C
|
|
|
ENST00000420124.2:c.6395G>C
|
ENSP00000398837.1:p.Arg2132Thr
|
|
NM_014727.2:c.6395G>C
|
NP_055542.1:p.Arg2132Thr
|
|
XM_011527561.1:c.6329G>C
|
XP_011525863.1:p.Arg2110Thr
|
|
XM_011527562.1:c.6395G>C
|
XP_011525864.1:p.Arg2132Thr
|
|
XM_011527563.1:c.6119G>C
|
XP_011525865.1:p.Arg2040Thr
|
|
XM_011527561.2:c.5831G>C
|
XP_011525863.2:p.Arg1944Thr
|
|
XM_011527562.2:c.6395G>C
|
XP_011525864.1:p.Arg2132Thr
|
|
XM_017027544.1:c.6395G>C
|
XP_016883033.1:p.Arg2132Thr
|
|
XM_017027545.1:c.5831G>C
|
XP_016883034.1:p.Arg1944Thr
|
|
XM_017027546.1:c.3359G>C
|
XP_016883035.1:p.Arg1120Thr
|
|
NM_014727.3:c.6395G>C
MANE Select
|
NP_055542.1:p.Arg2132Thr
|
|