ENST00000269980.7:c.727G>T
MANE Select
|
ENSP00000269980.2:p.Glu243Ter
|
|
ENST00000269980.6:c.727G>T
|
ENSP00000269980.2:p.Glu243Ter
|
|
ENST00000457836.6:c.661G>T
|
ENSP00000416000.2:p.Glu221Ter
|
|
ENST00000535632.5:n.356G>T
|
|
|
ENST00000540732.3:c.829G>T
|
ENSP00000443246.1:p.Glu277Ter
|
|
ENST00000541315.1:c.627G>T
|
|
|
ENST00000542943.5:c.640G>T
|
ENSP00000440345.1:p.Glu214Ter
|
|
ENST00000545787.1:n.355G>T
|
|
|
ENST00000595085.5:c.727G>T
|
ENSP00000471150.2:p.Glu243Ter
|
|
NM_000709.3:c.727G>T
|
NP_000700.1:p.Glu243Ter
|
|
NM_001164783.1:c.727G>T
|
NP_001158255.1:p.Glu243Ter
|
|
NM_000709.4:c.727G>T
MANE Select
|
NP_000700.1:p.Glu243Ter
|
|
NM_001164783.2:c.727G>T
|
NP_001158255.1:p.Glu243Ter
|
|