ENST00000269980.7:c.949G>C
MANE Select
|
ENSP00000269980.2:p.Ala317Pro
|
|
ENST00000269980.6:c.949G>C
|
ENSP00000269980.2:p.Ala317Pro
|
|
ENST00000457836.6:c.883G>C
|
ENSP00000416000.2:p.Ala295Pro
|
|
ENST00000535632.5:n.578G>C
|
|
|
ENST00000540732.3:c.1051G>C
|
ENSP00000443246.1:p.Ala351Pro
|
|
ENST00000542943.5:c.862G>C
|
ENSP00000440345.1:p.Ala288Pro
|
|
ENST00000545787.1:n.577G>C
|
|
|
ENST00000595085.5:c.922+27G>C
|
ENSP00000471150.2:n.922+27G>C
|
|
NM_000709.3:c.949G>C
|
NP_000700.1:p.Ala317Pro
|
|
NM_001164783.1:c.946G>C
|
NP_001158255.1:p.Ala316Pro
|
|
NM_000709.4:c.949G>C
MANE Select
|
NP_000700.1:p.Ala317Pro
|
|
NM_001164783.2:c.946G>C
|
NP_001158255.1:p.Ala316Pro
|
|