ENST00000269980.7:c.946C>A
MANE Select
|
ENSP00000269980.2:p.Arg316=
|
|
ENST00000269980.6:c.946C>A
|
ENSP00000269980.2:p.Arg316=
|
|
ENST00000457836.6:c.880C>A
|
ENSP00000416000.2:p.Arg294=
|
|
ENST00000535632.5:n.575C>A
|
|
|
ENST00000540732.3:c.1048C>A
|
ENSP00000443246.1:p.Arg350=
|
|
ENST00000542943.5:c.859C>A
|
ENSP00000440345.1:p.Arg287=
|
|
ENST00000545787.1:n.574C>A
|
|
|
ENST00000595085.5:c.922+24C>A
|
ENSP00000471150.2:n.922+24C>A
|
|
NM_000709.3:c.946C>A
|
NP_000700.1:p.Arg316=
|
|
NM_001164783.1:c.943C>A
|
NP_001158255.1:p.Arg315=
|
|
NM_000709.4:c.946C>A
MANE Select
|
NP_000700.1:p.Arg316=
|
|
NM_001164783.2:c.943C>A
|
NP_001158255.1:p.Arg315=
|
|