ENST00000463045.3:c.211T>C
|
ENSP00000481376.2:p.Tyr71His
|
|
ENST00000491274.6:c.340T>C
|
ENSP00000480482.2:p.Tyr114His
|
|
ENST00000375499.8:c.382T>C
MANE Select
|
ENSP00000364649.3:p.Tyr128His
|
|
ENST00000375499.7:c.382T>C
|
ENSP00000364649.3:p.Tyr128His
|
|
ENST00000463045.2:c.211T>C
|
ENSP00000481376.1:p.Tyr71His
|
|
ENST00000475506.1:n.299T>C
|
|
|
ENST00000485515.5:n.357+13T>C
|
|
|
ENST00000491274.5:c.340T>C
|
ENSP00000480482.1:p.Tyr114His
|
|
NM_003000.2:c.382T>C , LRG_316t1:c.382T>C
|
NP_002991.2:p.Tyr128His
|
|
NM_003000.3:c.382T>C
MANE Select
|
NP_002991.2:p.Tyr128His
|
|