ENST00000269980.7:c.688A>T
MANE Select
|
ENSP00000269980.2:p.Arg230Trp
|
|
ENST00000269980.6:c.688A>T
|
ENSP00000269980.2:p.Arg230Trp
|
|
ENST00000457836.6:c.622A>T
|
ENSP00000416000.2:p.Arg208Trp
|
|
ENST00000535632.5:n.317A>T
|
|
|
ENST00000538423.5:n.814A>T
|
|
|
ENST00000540732.3:c.790A>T
|
ENSP00000443246.1:p.Arg264Trp
|
|
ENST00000541315.1:c.588A>T
|
|
|
ENST00000542943.5:c.601A>T
|
ENSP00000440345.1:p.Arg201Trp
|
|
ENST00000545787.1:n.316A>T
|
|
|
ENST00000595085.5:c.688A>T
|
ENSP00000471150.2:p.Arg230Trp
|
|
NM_000709.3:c.688A>T
|
NP_000700.1:p.Arg230Trp
|
|
NM_001164783.1:c.688A>T
|
NP_001158255.1:p.Arg230Trp
|
|
NM_000709.4:c.688A>T
MANE Select
|
NP_000700.1:p.Arg230Trp
|
|
NM_001164783.2:c.688A>T
|
NP_001158255.1:p.Arg230Trp
|
|