ENST00000369538.4:c.1262G=
|
ENSP00000358551.4:p.Arg421=
|
|
ENST00000520113.7:c.1274G=
MANE Select
|
ENSP00000430075.3:p.Arg425=
|
|
ENST00000637080.1:c.1057G=
|
ENSP00000489753.1:n.1057G=
|
|
ENST00000639077.1:n.939G=
|
|
|
ENST00000369538.3:c.1361G=
|
ENSP00000358551.3:p.Arg454=
|
|
ENST00000520113.6:c.1373G=
|
ENSP00000430075.2:p.Arg458=
|
|
NM_000036.2:c.1373G=
|
NP_000027.2:p.Arg458=
|
|
NM_001172626.1:c.1361G=
|
NP_001166097.1:p.Arg454=
|
|
NM_000036.3:c.1274G=
MANE Select
|
NP_000027.3:p.Arg425=
|
|
NM_001172626.2:c.1262G=
|
NP_001166097.2:p.Arg421=
|
|