ENST00000269980.7:c.689G>C
MANE Select
|
ENSP00000269980.2:p.Arg230Thr
|
|
ENST00000269980.6:c.689G>C
|
ENSP00000269980.2:p.Arg230Thr
|
|
ENST00000457836.6:c.623G>C
|
ENSP00000416000.2:p.Arg208Thr
|
|
ENST00000535632.5:n.318G>C
|
|
|
ENST00000538423.5:n.815G>C
|
|
|
ENST00000540732.3:c.791G>C
|
ENSP00000443246.1:p.Arg264Thr
|
|
ENST00000541315.1:c.589G>C
|
|
|
ENST00000542943.5:c.602G>C
|
ENSP00000440345.1:p.Arg201Thr
|
|
ENST00000545787.1:n.317G>C
|
|
|
ENST00000595085.5:c.689G>C
|
ENSP00000471150.2:p.Arg230Thr
|
|
NM_000709.3:c.689G>C
|
NP_000700.1:p.Arg230Thr
|
|
NM_001164783.1:c.689G>C
|
NP_001158255.1:p.Arg230Thr
|
|
NM_000709.4:c.689G>C
MANE Select
|
NP_000700.1:p.Arg230Thr
|
|
NM_001164783.2:c.689G>C
|
NP_001158255.1:p.Arg230Thr
|
|