ENST00000269980.7:c.664G>T
MANE Select
|
ENSP00000269980.2:p.Ala222Ser
|
|
ENST00000269980.6:c.664G>T
|
ENSP00000269980.2:p.Ala222Ser
|
|
ENST00000457836.6:c.598G>T
|
ENSP00000416000.2:p.Ala200Ser
|
|
ENST00000535632.5:n.293G>T
|
|
|
ENST00000538423.5:n.790G>T
|
|
|
ENST00000540732.3:c.766G>T
|
ENSP00000443246.1:p.Ala256Ser
|
|
ENST00000541315.1:c.564G>T
|
|
|
ENST00000542943.5:c.577G>T
|
ENSP00000440345.1:p.Ala193Ser
|
|
ENST00000545787.1:n.292G>T
|
|
|
ENST00000595085.5:c.664G>T
|
ENSP00000471150.2:p.Ala222Ser
|
|
NM_000709.3:c.664G>T
|
NP_000700.1:p.Ala222Ser
|
|
NM_001164783.1:c.664G>T
|
NP_001158255.1:p.Ala222Ser
|
|
NM_000709.4:c.664G>T
MANE Select
|
NP_000700.1:p.Ala222Ser
|
|
NM_001164783.2:c.664G>T
|
NP_001158255.1:p.Ala222Ser
|
|