ENST00000269980.7:c.871T>A
MANE Select
|
ENSP00000269980.2:p.Tyr291Asn
|
|
ENST00000269980.6:c.871T>A
|
ENSP00000269980.2:p.Tyr291Asn
|
|
ENST00000457836.6:c.805T>A
|
ENSP00000416000.2:p.Tyr269Asn
|
|
ENST00000535632.5:n.500T>A
|
|
|
ENST00000540732.3:c.973T>A
|
ENSP00000443246.1:p.Tyr325Asn
|
|
ENST00000542943.5:c.784T>A
|
ENSP00000440345.1:p.Tyr262Asn
|
|
ENST00000545787.1:n.499T>A
|
|
|
ENST00000595085.5:c.871T>A
|
ENSP00000471150.2:p.Tyr291Asn
|
|
NM_000709.3:c.871T>A
|
NP_000700.1:p.Tyr291Asn
|
|
NM_001164783.1:c.868T>A
|
NP_001158255.1:p.Tyr290Asn
|
|
NM_000709.4:c.871T>A
MANE Select
|
NP_000700.1:p.Tyr291Asn
|
|
NM_001164783.2:c.868T>A
|
NP_001158255.1:p.Tyr290Asn
|
|