ENST00000357578.8:c.1283T>A
MANE Select
|
ENSP00000350191.3:p.Val428Asp
|
|
ENST00000479394.2:n.398T>A
|
|
|
ENST00000672352.1:c.902T>A
|
ENSP00000500876.1:p.Val301Asp
|
|
ENST00000672652.1:c.1246T>A
|
|
|
ENST00000348925.2:c.1322T>A
|
ENSP00000314649.3:p.Val441Asp
|
|
ENST00000357578.7:c.1283T>A
|
ENSP00000350191.3:p.Val428Asp
|
|
ENST00000479394.1:n.398T>A
|
|
|
ENST00000491546.5:c.1199T>A
|
ENSP00000417687.1:p.Val400Asp
|
|
NM_001080.3:c.1283T>A
MANE Select
|
NP_001071.1:p.Val428Asp
|
|
NM_170740.1:c.1322T>A
|
NP_733936.1:p.Val441Asp
|
|
NM_001368954.1:c.1139T>A
|
NP_001355883.1:p.Val380Asp
|
|