NM_000709.4:c.859C=
MANE Select
|
NP_000700.1:p.Arg287=
|
ENST00000269980.7:c.859C=
MANE Select
|
ENSP00000269980.2:p.Arg287=
|
NM_000709.3:c.859C=
|
NP_000700.1:p.Arg287=
|
NM_001164783.1:c.856C=
|
NP_001158255.1:p.Arg286=
|
NM_001164783.2:c.856C=
|
NP_001158255.1:p.Arg286=
|
ENST00000269980.6:c.859C=
|
ENSP00000269980.2:p.Arg287=
|
ENST00000457836.6:c.793C=
|
ENSP00000416000.2:p.Arg265=
|
ENST00000535632.5:n.488C=
|
|
ENST00000540732.3:c.961C=
|
ENSP00000443246.1:p.Arg321=
|
ENST00000542943.5:c.772C=
|
ENSP00000440345.1:p.Arg258=
|
ENST00000545787.1:n.487C=
|
|
ENST00000595085.5:c.859C=
|
ENSP00000471150.2:p.Arg287=
|