ENST00000357578.8:c.1316C=
MANE Select
|
ENSP00000350191.3:p.Thr439=
|
|
ENST00000479394.2:n.431C=
|
|
|
ENST00000672352.1:c.935C=
|
ENSP00000500876.1:p.Thr312=
|
|
ENST00000672652.1:c.1279C=
|
|
|
ENST00000348925.2:c.1355C=
|
ENSP00000314649.3:p.Thr452=
|
|
ENST00000357578.7:c.1316C=
|
ENSP00000350191.3:p.Thr439=
|
|
ENST00000479394.1:n.431C=
|
|
|
ENST00000491546.5:c.1232C=
|
ENSP00000417687.1:p.Thr411=
|
|
NM_001080.3:c.1316C=
MANE Select
|
NP_001071.1:p.Thr439=
|
|
NM_170740.1:c.1355C=
|
NP_733936.1:p.Thr452=
|
|
NM_001368954.1:c.1172C=
|
NP_001355883.1:p.Thr391=
|
|