ENST00000269980.7:c.1223T>A
MANE Select
|
ENSP00000269980.2:p.Leu408His
|
|
ENST00000269980.6:c.1223T>A
|
ENSP00000269980.2:p.Leu408His
|
|
ENST00000457836.6:c.1232T>A
|
ENSP00000416000.2:p.Leu411His
|
|
ENST00000540732.3:c.1325T>A
|
ENSP00000443246.1:p.Leu442His
|
|
ENST00000544905.1:c.62-9T>A
|
|
|
ENST00000595085.5:c.922+1796T>A
|
ENSP00000471150.2:n.922+1796T>A
|
|
NM_000709.3:c.1223T>A
|
NP_000700.1:p.Leu408His
|
|
NM_001164783.1:c.1220T>A
|
NP_001158255.1:p.Leu407His
|
|
NM_000709.4:c.1223T>A
MANE Select
|
NP_000700.1:p.Leu408His
|
|
NM_001164783.2:c.1220T>A
|
NP_001158255.1:p.Leu407His
|
|