ENST00000545712.7:c.678T>A
MANE Select
|
ENSP00000445920.1:p.Tyr226Ter
|
|
ENST00000537496.5:c.*243T>A
|
ENSP00000444793.1:n.*243T>A
|
|
ENST00000540016.5:c.522T>A
|
ENSP00000474582.1:p.Tyr174Ter
|
|
ENST00000541763.6:c.903T>A
|
ENSP00000474981.1:n.903T>A
|
|
ENST00000544051.5:c.*559T>A
|
ENSP00000438079.1:n.*559T>A
|
|
ENST00000545712.6:c.678T>A
|
ENSP00000445920.1:p.Tyr226Ter
|
|
NM_052845.3:c.678T>A
|
NP_443077.1:p.Tyr226Ter
|
|
NR_038118.1:n.838T>A
|
|
|
XM_011538266.1:c.*25T>A
|
XP_011536568.1:n.*25T>A
|
|
XM_011538267.1:c.*25T>A
|
XP_011536569.1:n.*25T>A
|
|
XM_011538268.1:c.405T>A
|
XP_011536570.1:p.Tyr135Ter
|
|
XM_011538269.1:c.402T>A
|
XP_011536571.1:p.Tyr134Ter
|
|
XM_011538267.3:c.*25T>A
|
XP_011536569.1:n.*25T>A
|
|
XM_011538268.2:c.405T>A
|
XP_011536570.1:p.Tyr135Ter
|
|
XM_011538269.2:c.402T>A
|
XP_011536571.1:p.Tyr134Ter
|
|
NM_052845.4:c.678T>A
MANE Select
|
NP_443077.1:p.Tyr226Ter
|
|
NR_038118.2:n.789T>A
|
|
|