ENST00000463045.3:c.218T>A
|
ENSP00000481376.2:p.Leu73His
|
|
ENST00000491274.6:c.347T>A
|
ENSP00000480482.2:p.Leu116His
|
|
ENST00000375499.8:c.389T>A
MANE Select
|
ENSP00000364649.3:p.Leu130His
|
|
ENST00000375499.7:c.389T>A
|
ENSP00000364649.3:p.Leu130His
|
|
ENST00000463045.2:c.218T>A
|
ENSP00000481376.1:p.Leu73His
|
|
ENST00000475506.1:n.306T>A
|
|
|
ENST00000485515.5:n.357+20T>A
|
|
|
ENST00000491274.5:c.347T>A
|
ENSP00000480482.1:p.Leu116His
|
|
NM_003000.2:c.389T>A , LRG_316t1:c.389T>A
|
NP_002991.2:p.Leu130His
|
|
NM_003000.3:c.389T>A
MANE Select
|
NP_002991.2:p.Leu130His
|
|