ENST00000545712.7:c.676T>C
MANE Select
|
ENSP00000445920.1:p.Tyr226His
|
|
ENST00000537496.5:c.*241T>C
|
ENSP00000444793.1:n.*241T>C
|
|
ENST00000540016.5:c.520T>C
|
ENSP00000474582.1:p.Tyr174His
|
|
ENST00000541763.6:c.901T>C
|
ENSP00000474981.1:n.901T>C
|
|
ENST00000544051.5:c.*557T>C
|
ENSP00000438079.1:n.*557T>C
|
|
ENST00000545712.6:c.676T>C
|
ENSP00000445920.1:p.Tyr226His
|
|
NM_052845.3:c.676T>C
|
NP_443077.1:p.Tyr226His
|
|
NR_038118.1:n.836T>C
|
|
|
XM_011538266.1:c.*23T>C
|
XP_011536568.1:n.*23T>C
|
|
XM_011538267.1:c.*23T>C
|
XP_011536569.1:n.*23T>C
|
|
XM_011538268.1:c.403T>C
|
XP_011536570.1:p.Tyr135His
|
|
XM_011538269.1:c.400T>C
|
XP_011536571.1:p.Tyr134His
|
|
XM_011538267.3:c.*23T>C
|
XP_011536569.1:n.*23T>C
|
|
XM_011538268.2:c.403T>C
|
XP_011536570.1:p.Tyr135His
|
|
XM_011538269.2:c.400T>C
|
XP_011536571.1:p.Tyr134His
|
|
NM_052845.4:c.676T>C
MANE Select
|
NP_443077.1:p.Tyr226His
|
|
NR_038118.2:n.787T>C
|
|
|