ENST00000357578.8:c.1282G=
MANE Select
|
ENSP00000350191.3:p.Val428=
|
|
ENST00000479394.2:n.397G=
|
|
|
ENST00000672352.1:c.901G=
|
ENSP00000500876.1:p.Val301=
|
|
ENST00000672652.1:c.1245G=
|
|
|
ENST00000348925.2:c.1321G=
|
ENSP00000314649.3:p.Val441=
|
|
ENST00000357578.7:c.1282G=
|
ENSP00000350191.3:p.Val428=
|
|
ENST00000479394.1:n.397G=
|
|
|
ENST00000491546.5:c.1198G=
|
ENSP00000417687.1:p.Val400=
|
|
NM_001080.3:c.1282G=
MANE Select
|
NP_001071.1:p.Val428=
|
|
NM_170740.1:c.1321G=
|
NP_733936.1:p.Val441=
|
|
NM_001368954.1:c.1138G=
|
NP_001355883.1:p.Val380=
|
|