ENST00000269980.7:c.1293G>T
MANE Select
|
ENSP00000269980.2:p.Leu431=
|
|
ENST00000269980.6:c.1293G>T
|
ENSP00000269980.2:p.Leu431=
|
|
ENST00000457836.6:c.1302G>T
|
ENSP00000416000.2:p.Leu434=
|
|
ENST00000540732.3:c.1395G>T
|
ENSP00000443246.1:p.Leu465=
|
|
ENST00000544905.1:c.123G>T
|
|
|
ENST00000595085.5:c.922+1866G>T
|
ENSP00000471150.2:n.922+1866G>T
|
|
NM_000709.3:c.1293G>T
|
NP_000700.1:p.Leu431=
|
|
NM_001164783.1:c.1290G>T
|
NP_001158255.1:p.Leu430=
|
|
NM_000709.4:c.1293G>T
MANE Select
|
NP_000700.1:p.Leu431=
|
|
NM_001164783.2:c.1290G>T
|
NP_001158255.1:p.Leu430=
|
|