ENST00000463045.3:c.298T>G
|
ENSP00000481376.2:p.Leu100Val
|
|
ENST00000491274.6:c.427T>G
|
ENSP00000480482.2:p.Leu143Val
|
|
ENST00000375499.8:c.469T>G
MANE Select
|
ENSP00000364649.3:p.Leu157Val
|
|
ENST00000375499.7:c.469T>G
|
ENSP00000364649.3:p.Leu157Val
|
|
ENST00000463045.2:c.298T>G
|
ENSP00000481376.1:p.Leu100Val
|
|
ENST00000475506.1:n.386T>G
|
|
|
ENST00000485515.5:n.403T>G
|
|
|
ENST00000491274.5:c.427T>G
|
ENSP00000480482.1:p.Leu143Val
|
|
NM_003000.2:c.469T>G , LRG_316t1:c.469T>G
|
NP_002991.2:p.Leu157Val
|
|
NM_003000.3:c.469T>G
MANE Select
|
NP_002991.2:p.Leu157Val
|
|