ENST00000357578.8:c.1267A=
MANE Select
|
ENSP00000350191.3:p.Thr423=
|
|
ENST00000479394.2:n.382A=
|
|
|
ENST00000672352.1:c.886A=
|
ENSP00000500876.1:p.Thr296=
|
|
ENST00000672652.1:c.1230A=
|
|
|
ENST00000348925.2:c.1306A=
|
ENSP00000314649.3:p.Thr436=
|
|
ENST00000357578.7:c.1267A=
|
ENSP00000350191.3:p.Thr423=
|
|
ENST00000479394.1:n.382A=
|
|
|
ENST00000491546.5:c.1183A=
|
ENSP00000417687.1:p.Thr395=
|
|
NM_001080.3:c.1267A=
MANE Select
|
NP_001071.1:p.Thr423=
|
|
NM_170740.1:c.1306A=
|
NP_733936.1:p.Thr436=
|
|
NM_001368954.1:c.1123A=
|
NP_001355883.1:p.Thr375=
|
|