ENST00000357578.8:c.1307A>G
MANE Select
|
ENSP00000350191.3:p.His436Arg
|
|
ENST00000479394.2:n.422A>G
|
|
|
ENST00000672352.1:c.926A>G
|
ENSP00000500876.1:p.His309Arg
|
|
ENST00000672652.1:c.1270A>G
|
|
|
ENST00000348925.2:c.1346A>G
|
ENSP00000314649.3:p.His449Arg
|
|
ENST00000357578.7:c.1307A>G
|
ENSP00000350191.3:p.His436Arg
|
|
ENST00000479394.1:n.422A>G
|
|
|
ENST00000491546.5:c.1223A>G
|
ENSP00000417687.1:p.His408Arg
|
|
NM_001080.3:c.1307A>G
MANE Select
|
NP_001071.1:p.His436Arg
|
|
NM_170740.1:c.1346A>G
|
NP_733936.1:p.His449Arg
|
|
NM_001368954.1:c.1163A>G
|
NP_001355883.1:p.His388Arg
|
|