ENST00000463045.3:c.-89G>T
|
ENSP00000481376.2:n.-89G>T
|
|
ENST00000491274.6:c.41G>T
|
ENSP00000480482.2:p.Gly14Val
|
|
ENST00000375499.8:c.83G>T
MANE Select
|
ENSP00000364649.3:p.Gly28Val
|
|
ENST00000375499.7:c.83G>T
|
ENSP00000364649.3:p.Gly28Val
|
|
ENST00000463045.2:c.-89G>T
|
ENSP00000481376.1:n.-89G>T
|
|
ENST00000466613.2:n.95G>T
|
|
|
ENST00000485515.5:n.71G>T
|
|
|
ENST00000491274.5:c.41G>T
|
ENSP00000480482.1:p.Gly14Val
|
|
NM_003000.2:c.83G>T , LRG_316t1:c.83G>T
|
NP_002991.2:p.Gly28Val
|
|
NM_003000.3:c.83G>T
MANE Select
|
NP_002991.2:p.Gly28Val
|
|