ENST00000625662.3:c.2093T>A
|
|
|
ENST00000628118.2:c.1620T>A
|
|
|
ENST00000700551.1:c.*1417T>A
|
ENSP00000515057.1:n.*1417T>A
|
|
ENST00000394196.9:c.2586T>A
MANE Select
|
ENSP00000377747.4:p.Cys862Ter
|
|
ENST00000635856.1:n.3158T>A
|
|
|
ENST00000636306.1:n.146T>A
|
|
|
ENST00000636881.1:c.1957T>A
|
|
|
ENST00000637572.1:n.3330T>A
|
|
|
ENST00000394196.8:c.2586T>A
|
ENSP00000377747.4:p.Cys862Ter
|
|
ENST00000625463.1:c.126T>A
|
ENSP00000486391.1:p.Cys42Ter
|
|
ENST00000626874.2:c.2586T>A
|
ENSP00000486629.1:p.Cys862Ter
|
|
ENST00000628118.1:n.365T>A
|
|
|
NM_001271.3:c.2586T>A
|
NP_001262.3:p.Cys862Ter
|
|
NM_001271.4:c.2586T>A
MANE Select
|
NP_001262.3:p.Cys862Ter
|
|