ENST00000625662.3:c.2089T>G
|
|
|
ENST00000628118.2:c.1616T>G
|
|
|
ENST00000700551.1:c.*1413T>G
|
ENSP00000515057.1:n.*1413T>G
|
|
ENST00000394196.9:c.2582T>G
MANE Select
|
ENSP00000377747.4:p.Phe861Cys
|
|
ENST00000635856.1:n.3154T>G
|
|
|
ENST00000636306.1:n.142T>G
|
|
|
ENST00000636881.1:c.1953T>G
|
|
|
ENST00000637572.1:n.3326T>G
|
|
|
ENST00000394196.8:c.2582T>G
|
ENSP00000377747.4:p.Phe861Cys
|
|
ENST00000625463.1:c.122T>G
|
ENSP00000486391.1:p.Phe41Cys
|
|
ENST00000626874.2:c.2582T>G
|
ENSP00000486629.1:p.Phe861Cys
|
|
ENST00000628118.1:n.361T>G
|
|
|
NM_001271.3:c.2582T>G
|
NP_001262.3:p.Phe861Cys
|
|
NM_001271.4:c.2582T>G
MANE Select
|
NP_001262.3:p.Phe861Cys
|
|