|
NM_001080.3:c.1268C>G
MANE Select
|
NP_001071.1:p.Thr423Ser
|
|
ENST00000357578.8:c.1268C>G
MANE Select
|
ENSP00000350191.3:p.Thr423Ser
|
|
NM_001368954.1:c.1124C>G
|
NP_001355883.1:p.Thr375Ser
|
|
NM_170740.1:c.1307C>G
|
NP_733936.1:p.Thr436Ser
|
|
ENST00000348925.2:c.1307C>G
|
ENSP00000314649.3:p.Thr436Ser
|
|
ENST00000357578.7:c.1268C>G
|
ENSP00000350191.3:p.Thr423Ser
|
|
ENST00000479394.1:n.383C>G
|
|
|
ENST00000479394.2:n.383C>G
|
|
|
ENST00000491546.5:c.1184C>G
|
ENSP00000417687.1:p.Thr395Ser
|
|
ENST00000672352.1:c.887C>G
|
ENSP00000500876.1:p.Thr296Ser
|
|
ENST00000672652.1:c.1231C>G
|
|