|
NM_001080.3:c.1592G>A
MANE Select
|
NP_001071.1:p.Cys531Tyr
|
|
ENST00000357578.8:c.1592G>A
MANE Select
|
ENSP00000350191.3:p.Cys531Tyr
|
|
NM_001368954.1:c.1448G>A
|
NP_001355883.1:p.Cys483Tyr
|
|
NM_170740.1:c.1631G>A
|
NP_733936.1:p.Cys544Tyr
|
|
ENST00000348925.2:c.1631G>A
|
ENSP00000314649.3:p.Cys544Tyr
|
|
ENST00000357578.7:c.1592G>A
|
ENSP00000350191.3:p.Cys531Tyr
|
|
ENST00000479394.1:n.707G>A
|
|
|
ENST00000479394.2:n.707G>A
|
|
|
ENST00000491546.5:c.1508G>A
|
ENSP00000417687.1:p.Cys503Tyr
|
|
ENST00000492697.1:n.358G>A
|
|
|
ENST00000672352.1:c.1211G>A
|
ENSP00000500876.1:p.Cys404Tyr
|
|
ENST00000672652.1:c.1555G>A
|
|