ENST00000237014.8:c.329A>G
MANE Select
|
ENSP00000237014.4:p.His110Arg
|
|
ENST00000610404.5:c.233A>G
|
ENSP00000477599.2:p.His78Arg
|
|
ENST00000649620.1:c.329A>G
|
ENSP00000497927.1:p.His110Arg
|
|
ENST00000237014.7:c.329A>G
|
ENSP00000237014.3:p.His110Arg
|
|
ENST00000541025.2:n.355A>G
|
|
|
ENST00000610404.4:c.329A>G
|
ENSP00000477599.1:p.His110Arg
|
|
ENST00000613781.1:c.329A>G
|
ENSP00000479174.1:p.His110Arg
|
|
NM_000371.3:c.329A>G , LRG_416t1:c.329A>G
|
NP_000362.1:p.His110Arg
|
|
NM_000371.4:c.329A>G
MANE Select
|
NP_000362.1:p.His110Arg
|
|