ENST00000269980.7:c.726T>G
MANE Select
|
ENSP00000269980.2:p.Ser242Arg
|
|
ENST00000269980.6:c.726T>G
|
ENSP00000269980.2:p.Ser242Arg
|
|
ENST00000457836.6:c.660T>G
|
ENSP00000416000.2:p.Ser220Arg
|
|
ENST00000535632.5:n.355T>G
|
|
|
ENST00000540732.3:c.828T>G
|
ENSP00000443246.1:p.Ser276Arg
|
|
ENST00000541315.1:c.626T>G
|
|
|
ENST00000542943.5:c.639T>G
|
ENSP00000440345.1:p.Ser213Arg
|
|
ENST00000545787.1:n.354T>G
|
|
|
ENST00000595085.5:c.726T>G
|
ENSP00000471150.2:p.Ser242Arg
|
|
NM_000709.3:c.726T>G
|
NP_000700.1:p.Ser242Arg
|
|
NM_001164783.1:c.726T>G
|
NP_001158255.1:p.Ser242Arg
|
|
NM_000709.4:c.726T>G
MANE Select
|
NP_000700.1:p.Ser242Arg
|
|
NM_001164783.2:c.726T>G
|
NP_001158255.1:p.Ser242Arg
|
|