ENST00000269980.7:c.840C>A
MANE Select
|
ENSP00000269980.2:p.Arg280=
|
|
ENST00000269980.6:c.840C>A
|
ENSP00000269980.2:p.Arg280=
|
|
ENST00000457836.6:c.774C>A
|
ENSP00000416000.2:p.Arg258=
|
|
ENST00000535632.5:n.469C>A
|
|
|
ENST00000540732.3:c.942C>A
|
ENSP00000443246.1:p.Arg314=
|
|
ENST00000542943.5:c.753C>A
|
ENSP00000440345.1:p.Arg251=
|
|
ENST00000545787.1:n.468C>A
|
|
|
ENST00000595085.5:c.840C>A
|
ENSP00000471150.2:p.Arg280=
|
|
NM_000709.3:c.840C>A
|
NP_000700.1:p.Arg280=
|
|
NM_001164783.1:c.840C>A
|
NP_001158255.1:p.Arg280=
|
|
NM_000709.4:c.840C>A
MANE Select
|
NP_000700.1:p.Arg280=
|
|
NM_001164783.2:c.840C>A
|
NP_001158255.1:p.Arg280=
|
|