ENST00000269980.7:c.687C>T
MANE Select
|
ENSP00000269980.2:p.Asn229=
|
|
ENST00000269980.6:c.687C>T
|
ENSP00000269980.2:p.Asn229=
|
|
ENST00000457836.6:c.621C>T
|
ENSP00000416000.2:p.Asn207=
|
|
ENST00000535632.5:n.316C>T
|
|
|
ENST00000538423.5:n.813C>T
|
|
|
ENST00000540732.3:c.789C>T
|
ENSP00000443246.1:p.Asn263=
|
|
ENST00000541315.1:c.587C>T
|
|
|
ENST00000542943.5:c.600C>T
|
ENSP00000440345.1:p.Asn200=
|
|
ENST00000545787.1:n.315C>T
|
|
|
ENST00000595085.5:c.687C>T
|
ENSP00000471150.2:p.Asn229=
|
|
NM_000709.3:c.687C>T
|
NP_000700.1:p.Asn229=
|
|
NM_001164783.1:c.687C>T
|
NP_001158255.1:p.Asn229=
|
|
NM_000709.4:c.687C>T
MANE Select
|
NP_000700.1:p.Asn229=
|
|
NM_001164783.2:c.687C>T
|
NP_001158255.1:p.Asn229=
|
|