ENST00000348974.5:c.949T>G
|
ENSP00000330021.7:p.Leu317Val
|
|
ENST00000394236.9:c.949T>G
MANE Select
|
ENSP00000377783.3:p.Leu317Val
|
|
ENST00000407433.6:c.904T>G
|
ENSP00000385794.2:p.Leu302Val
|
|
ENST00000647936.1:c.949T>G
|
ENSP00000496822.1:p.Leu317Val
|
|
ENST00000648381.1:n.1117T>G
|
|
|
ENST00000648853.1:c.907T>G
|
ENSP00000497262.1:p.Leu303Val
|
|
ENST00000649103.1:c.1048T>G
|
ENSP00000497962.1:n.1048T>G
|
|
ENST00000650591.1:c.1045T>G
|
ENSP00000497376.1:p.Leu349Val
|
|
ENST00000394236.7:c.949T>G
|
ENSP00000377783.3:p.Leu317Val
|
|
ENST00000407433.5:c.556T>G
|
ENSP00000385794.1:p.Leu186Val
|
|
NM_000313.3:c.949T>G , LRG_572t1:c.949T>G
|
NP_000304.2:p.Leu317Val
|
|
NM_001314077.1:c.1045T>G , LRG_572t2:c.1045T>G
|
NP_001301006.1:p.Leu349Val
|
|
NM_000313.4:c.949T>G
MANE Select
|
NP_000304.2:p.Leu317Val
|
|
NM_001314077.2:c.1045T>G
|
NP_001301006.1:p.Leu349Val
|
|