ENST00000269980.7:c.753C>T
MANE Select
|
ENSP00000269980.2:p.Asn251=
|
|
ENST00000269980.6:c.753C>T
|
ENSP00000269980.2:p.Asn251=
|
|
ENST00000457836.6:c.687C>T
|
ENSP00000416000.2:p.Asn229=
|
|
ENST00000535632.5:n.382C>T
|
|
|
ENST00000540732.3:c.855C>T
|
ENSP00000443246.1:p.Asn285=
|
|
ENST00000542943.5:c.666C>T
|
ENSP00000440345.1:p.Asn222=
|
|
ENST00000545787.1:n.381C>T
|
|
|
ENST00000595085.5:c.753C>T
|
ENSP00000471150.2:p.Asn251=
|
|
NM_000709.3:c.753C>T
|
NP_000700.1:p.Asn251=
|
|
NM_001164783.1:c.753C>T
|
NP_001158255.1:p.Asn251=
|
|
NM_000709.4:c.753C>T
MANE Select
|
NP_000700.1:p.Asn251=
|
|
NM_001164783.2:c.753C>T
|
NP_001158255.1:p.Asn251=
|
|