|
ENST00000682775.1:c.1342C>G
|
ENSP00000508399.1:p.Leu448Val
|
|
|
ENST00000682944.1:c.1342C>G
|
ENSP00000507173.1:p.Leu448Val
|
|
|
ENST00000683154.1:n.1480C>G
|
|
|
|
ENST00000683210.1:c.1342C>G
|
ENSP00000506739.1:p.Leu448Val
|
|
|
ENST00000683270.1:c.1333C>G
|
ENSP00000507624.1:p.Leu445Val
|
|
|
ENST00000683367.1:c.1333C>G
|
ENSP00000507780.1:p.Leu445Val
|
|
|
ENST00000683489.1:c.1342C>G
|
ENSP00000508403.1:p.Leu448Val
|
|
|
ENST00000683680.1:c.1342C>G
|
ENSP00000507223.1:p.Leu448Val
|
|
|
ENST00000684163.1:c.1333C>G
|
ENSP00000508262.1:p.Leu445Val
|
|
|
ENST00000684196.1:n.3699C>G
|
|
|
|
ENST00000684325.1:c.1342C>G
|
ENSP00000508121.1:p.Leu448Val
|
|
|
ENST00000684385.1:c.1342C>G
|
ENSP00000507855.1:p.Leu448Val
|
|
|
ENST00000684497.1:c.1342C>G
|
ENSP00000507057.1:p.Leu448Val
|
|
|
ENST00000382292.9:c.1342C>G
MANE Select
|
ENSP00000371729.3:p.Leu448Val
|
|
|
ENST00000423156.2:c.1342C>G
|
ENSP00000390925.2:p.Leu448Val
|
|
|
ENST00000455470.6:c.1342C>G
|
ENSP00000406565.2:p.Leu448Val
|
|
|
ENST00000382292.7:c.1342C>G
|
ENSP00000371729.3:p.Leu448Val
|
|
|
ENST00000382298.7:c.1342C>G
|
ENSP00000371735.3:p.Leu448Val
|
|
|
ENST00000402364.1:c.-909C>G
|
ENSP00000385844.1:n.-909C>G
|
|
|
ENST00000423156.1:c.214C>G
|
ENSP00000390925.1:p.Leu72Val
|
|
|
ENST00000455470.5:c.1040C>G
|
|
|
|
NM_001278055.1:c.901C>G
|
NP_001264984.1:p.Leu301Val
|
|
|
NM_014363.5:c.1342C>G
|
NP_055178.3:p.Leu448Val
|
|
|
XM_005266338.1:c.1342C>G
|
XP_005266395.1:p.Leu448Val
|
|
|
XM_011535038.1:c.1366C>G
|
XP_011533340.1:p.Leu456Val
|
|
|
XM_011535039.1:c.1333C>G
|
XP_011533341.1:p.Leu445Val
|
|
|
XM_005266338.2:c.1342C>G
|
XP_005266395.1:p.Leu448Val
|
|
|
XM_011535039.2:c.1333C>G
|
XP_011533341.1:p.Leu445Val
|
|
|
XM_017020539.1:c.1333C>G
|
XP_016876028.1:p.Leu445Val
|
|
|
XM_024449337.1:c.1342C>G
|
XP_024305105.1:p.Leu448Val
|
|
|
NM_014363.6:c.1342C>G
MANE Select
|
NP_055178.3:p.Leu448Val
|
|
|
NM_001278055.2:c.901C>G
|
NP_001264984.1:p.Leu301Val
|
|
