ENST00000269980.7:c.768T>G
MANE Select
|
ENSP00000269980.2:p.Leu256=
|
|
ENST00000269980.6:c.768T>G
|
ENSP00000269980.2:p.Leu256=
|
|
ENST00000457836.6:c.702T>G
|
ENSP00000416000.2:p.Leu234=
|
|
ENST00000535632.5:n.397T>G
|
|
|
ENST00000540732.3:c.870T>G
|
ENSP00000443246.1:p.Leu290=
|
|
ENST00000542943.5:c.681T>G
|
ENSP00000440345.1:p.Leu227=
|
|
ENST00000545787.1:n.396T>G
|
|
|
ENST00000595085.5:c.768T>G
|
ENSP00000471150.2:p.Leu256=
|
|
NM_000709.3:c.768T>G
|
NP_000700.1:p.Leu256=
|
|
NM_001164783.1:c.768T>G
|
NP_001158255.1:p.Leu256=
|
|
NM_000709.4:c.768T>G
MANE Select
|
NP_000700.1:p.Leu256=
|
|
NM_001164783.2:c.768T>G
|
NP_001158255.1:p.Leu256=
|
|