ENST00000269980.7:c.895G>A
MANE Select
|
ENSP00000269980.2:p.Asp299Asn
|
|
ENST00000269980.6:c.895G>A
|
ENSP00000269980.2:p.Asp299Asn
|
|
ENST00000457836.6:c.829G>A
|
ENSP00000416000.2:p.Asp277Asn
|
|
ENST00000535632.5:n.524G>A
|
|
|
ENST00000540732.3:c.997G>A
|
ENSP00000443246.1:p.Asp333Asn
|
|
ENST00000542943.5:c.808G>A
|
ENSP00000440345.1:p.Asp270Asn
|
|
ENST00000545787.1:n.523G>A
|
|
|
ENST00000595085.5:c.895G>A
|
ENSP00000471150.2:p.Asp299Asn
|
|
NM_000709.3:c.895G>A
|
NP_000700.1:p.Asp299Asn
|
|
NM_001164783.1:c.892G>A
|
NP_001158255.1:p.Asp298Asn
|
|
NM_000709.4:c.895G>A
MANE Select
|
NP_000700.1:p.Asp299Asn
|
|
NM_001164783.2:c.892G>A
|
NP_001158255.1:p.Asp298Asn
|
|