ENST00000269980.7:c.280G>T
MANE Select
|
ENSP00000269980.2:p.Asp94Tyr
|
|
ENST00000269980.6:c.280G>T
|
ENSP00000269980.2:p.Asp94Tyr
|
|
ENST00000457836.6:c.214G>T
|
ENSP00000416000.2:p.Asp72Tyr
|
|
ENST00000538423.5:n.300G>T
|
|
|
ENST00000540732.3:c.382G>T
|
ENSP00000443246.1:p.Asp128Tyr
|
|
ENST00000541315.1:c.87G>T
|
|
|
ENST00000542943.5:c.280G>T
|
ENSP00000440345.1:p.Asp94Tyr
|
|
ENST00000595085.5:c.280G>T
|
ENSP00000471150.2:p.Asp94Tyr
|
|
ENST00000604424.1:n.522G>T
|
|
|
NM_000709.3:c.280G>T
|
NP_000700.1:p.Asp94Tyr
|
|
NM_001164783.1:c.280G>T
|
NP_001158255.1:p.Asp94Tyr
|
|
NM_000709.4:c.280G>T
MANE Select
|
NP_000700.1:p.Asp94Tyr
|
|
NM_001164783.2:c.280G>T
|
NP_001158255.1:p.Asp94Tyr
|
|