ENST00000348974.5:c.937T>G
|
ENSP00000330021.7:p.Leu313Val
|
|
ENST00000394236.9:c.937T>G
MANE Select
|
ENSP00000377783.3:p.Leu313Val
|
|
ENST00000407433.6:c.892T>G
|
ENSP00000385794.2:p.Leu298Val
|
|
ENST00000647936.1:c.937T>G
|
ENSP00000496822.1:p.Leu313Val
|
|
ENST00000648381.1:n.1105T>G
|
|
|
ENST00000648853.1:c.895T>G
|
ENSP00000497262.1:p.Leu299Val
|
|
ENST00000649103.1:c.1036T>G
|
ENSP00000497962.1:n.1036T>G
|
|
ENST00000650591.1:c.1033T>G
|
ENSP00000497376.1:p.Leu345Val
|
|
ENST00000394236.7:c.937T>G
|
ENSP00000377783.3:p.Leu313Val
|
|
ENST00000407433.5:c.544T>G
|
ENSP00000385794.1:p.Leu182Val
|
|
NM_000313.3:c.937T>G , LRG_572t1:c.937T>G
|
NP_000304.2:p.Leu313Val
|
|
NM_001314077.1:c.1033T>G , LRG_572t2:c.1033T>G
|
NP_001301006.1:p.Leu345Val
|
|
NM_000313.4:c.937T>G
MANE Select
|
NP_000304.2:p.Leu313Val
|
|
NM_001314077.2:c.1033T>G
|
NP_001301006.1:p.Leu345Val
|
|