ENST00000269980.7:c.1237T>C
MANE Select
|
ENSP00000269980.2:p.Tyr413His
|
|
ENST00000269980.6:c.1237T>C
|
ENSP00000269980.2:p.Tyr413His
|
|
ENST00000457836.6:c.1246T>C
|
ENSP00000416000.2:p.Tyr416His
|
|
ENST00000540732.3:c.1339T>C
|
ENSP00000443246.1:p.Tyr447His
|
|
ENST00000544905.1:c.67T>C
|
|
|
ENST00000595085.5:c.922+1810T>C
|
ENSP00000471150.2:n.922+1810T>C
|
|
NM_000709.3:c.1237T>C
|
NP_000700.1:p.Tyr413His
|
|
NM_001164783.1:c.1234T>C
|
NP_001158255.1:p.Tyr412His
|
|
NM_000709.4:c.1237T>C
MANE Select
|
NP_000700.1:p.Tyr413His
|
|
NM_001164783.2:c.1234T>C
|
NP_001158255.1:p.Tyr412His
|
|