ENST00000269980.7:c.668C>T
MANE Select
|
ENSP00000269980.2:p.Ala223Val
|
|
ENST00000269980.6:c.668C>T
|
ENSP00000269980.2:p.Ala223Val
|
|
ENST00000457836.6:c.602C>T
|
ENSP00000416000.2:p.Ala201Val
|
|
ENST00000535632.5:n.297C>T
|
|
|
ENST00000538423.5:n.794C>T
|
|
|
ENST00000540732.3:c.770C>T
|
ENSP00000443246.1:p.Ala257Val
|
|
ENST00000541315.1:c.568C>T
|
|
|
ENST00000542943.5:c.581C>T
|
ENSP00000440345.1:p.Ala194Val
|
|
ENST00000545787.1:n.296C>T
|
|
|
ENST00000595085.5:c.668C>T
|
ENSP00000471150.2:p.Ala223Val
|
|
NM_000709.3:c.668C>T
|
NP_000700.1:p.Ala223Val
|
|
NM_001164783.1:c.668C>T
|
NP_001158255.1:p.Ala223Val
|
|
NM_000709.4:c.668C>T
MANE Select
|
NP_000700.1:p.Ala223Val
|
|
NM_001164783.2:c.668C>T
|
NP_001158255.1:p.Ala223Val
|
|