ENST00000369538.4:c.1334A>G
|
ENSP00000358551.4:p.His445Arg
|
|
ENST00000520113.7:c.1346A>G
MANE Select
|
ENSP00000430075.3:p.His449Arg
|
|
ENST00000637080.1:c.1129A>G
|
ENSP00000489753.1:n.1129A>G
|
|
ENST00000639077.1:n.1011A>G
|
|
|
ENST00000369538.3:c.1433A>G
|
ENSP00000358551.3:p.His478Arg
|
|
ENST00000520113.6:c.1445A>G
|
ENSP00000430075.2:p.His482Arg
|
|
NM_000036.2:c.1445A>G
|
NP_000027.2:p.His482Arg
|
|
NM_001172626.1:c.1433A>G
|
NP_001166097.1:p.His478Arg
|
|
NM_000036.3:c.1346A>G
MANE Select
|
NP_000027.3:p.His449Arg
|
|
NM_001172626.2:c.1334A>G
|
NP_001166097.2:p.His445Arg
|
|