ENST00000269980.7:c.766C>G
MANE Select
|
ENSP00000269980.2:p.Leu256Val
|
|
ENST00000269980.6:c.766C>G
|
ENSP00000269980.2:p.Leu256Val
|
|
ENST00000457836.6:c.700C>G
|
ENSP00000416000.2:p.Leu234Val
|
|
ENST00000535632.5:n.395C>G
|
|
|
ENST00000540732.3:c.868C>G
|
ENSP00000443246.1:p.Leu290Val
|
|
ENST00000542943.5:c.679C>G
|
ENSP00000440345.1:p.Leu227Val
|
|
ENST00000545787.1:n.394C>G
|
|
|
ENST00000595085.5:c.766C>G
|
ENSP00000471150.2:p.Leu256Val
|
|
NM_000709.3:c.766C>G
|
NP_000700.1:p.Leu256Val
|
|
NM_001164783.1:c.766C>G
|
NP_001158255.1:p.Leu256Val
|
|
NM_000709.4:c.766C>G
MANE Select
|
NP_000700.1:p.Leu256Val
|
|
NM_001164783.2:c.766C>G
|
NP_001158255.1:p.Leu256Val
|
|