ENST00000269980.7:c.792C>G
MANE Select
|
ENSP00000269980.2:p.Cys264Trp
|
|
ENST00000269980.6:c.792C>G
|
ENSP00000269980.2:p.Cys264Trp
|
|
ENST00000457836.6:c.726C>G
|
ENSP00000416000.2:p.Cys242Trp
|
|
ENST00000535632.5:n.421C>G
|
|
|
ENST00000540732.3:c.894C>G
|
ENSP00000443246.1:p.Cys298Trp
|
|
ENST00000542943.5:c.705C>G
|
ENSP00000440345.1:p.Cys235Trp
|
|
ENST00000545787.1:n.420C>G
|
|
|
ENST00000595085.5:c.792C>G
|
ENSP00000471150.2:p.Cys264Trp
|
|
NM_000709.3:c.792C>G
|
NP_000700.1:p.Cys264Trp
|
|
NM_001164783.1:c.792C>G
|
NP_001158255.1:p.Cys264Trp
|
|
NM_000709.4:c.792C>G
MANE Select
|
NP_000700.1:p.Cys264Trp
|
|
NM_001164783.2:c.792C>G
|
NP_001158255.1:p.Cys264Trp
|
|