ENST00000545712.7:c.566G>A
MANE Select
|
ENSP00000445920.1:p.Cys189Tyr
|
|
ENST00000537496.5:c.*131G>A
|
ENSP00000444793.1:n.*131G>A
|
|
ENST00000540016.5:c.410G>A
|
ENSP00000474582.1:p.Cys137Tyr
|
|
ENST00000541763.6:c.791G>A
|
ENSP00000474981.1:n.791G>A
|
|
ENST00000544051.5:c.*447G>A
|
ENSP00000438079.1:n.*447G>A
|
|
ENST00000545712.6:c.566G>A
|
ENSP00000445920.1:p.Cys189Tyr
|
|
NM_052845.3:c.566G>A
|
NP_443077.1:p.Cys189Tyr
|
|
NR_038118.1:n.726G>A
|
|
|
XM_011538266.1:c.411G>A
|
XP_011536568.1:p.Val137=
|
|
XM_011538267.1:c.411G>A
|
XP_011536569.1:p.Val137=
|
|
XM_011538268.1:c.293G>A
|
XP_011536570.1:p.Cys98Tyr
|
|
XM_011538269.1:c.290G>A
|
XP_011536571.1:p.Cys97Tyr
|
|
XM_011538267.3:c.411G>A
|
XP_011536569.1:p.Val137=
|
|
XM_011538268.2:c.293G>A
|
XP_011536570.1:p.Cys98Tyr
|
|
XM_011538269.2:c.290G>A
|
XP_011536571.1:p.Cys97Tyr
|
|
XM_024448961.1:c.566G>A
|
XP_024304729.1:p.Cys189Tyr
|
|
NM_052845.4:c.566G>A
MANE Select
|
NP_443077.1:p.Cys189Tyr
|
|
NR_038118.2:n.677G>A
|
|
|