ENST00000463045.3:c.55T>G
|
ENSP00000481376.2:p.Leu19Val
|
|
ENST00000491274.6:c.184T>G
|
ENSP00000480482.2:p.Leu62Val
|
|
ENST00000375499.8:c.226T>G
MANE Select
|
ENSP00000364649.3:p.Leu76Val
|
|
ENST00000375499.7:c.226T>G
|
ENSP00000364649.3:p.Leu76Val
|
|
ENST00000463045.2:c.55T>G
|
ENSP00000481376.1:p.Leu19Val
|
|
ENST00000466613.2:n.238T>G
|
|
|
ENST00000475506.1:n.143T>G
|
|
|
ENST00000485515.5:n.214T>G
|
|
|
ENST00000491274.5:c.184T>G
|
ENSP00000480482.1:p.Leu62Val
|
|
NM_003000.2:c.226T>G , LRG_316t1:c.226T>G
|
NP_002991.2:p.Leu76Val
|
|
NM_003000.3:c.226T>G
MANE Select
|
NP_002991.2:p.Leu76Val
|
|