ENST00000527168.6:n.599T>G
|
|
|
ENST00000529110.2:c.584T>G
|
ENSP00000435349.2:p.Leu195Arg
|
|
ENST00000529957.6:n.558T>G
|
|
|
ENST00000683366.1:c.*232T>G
|
ENSP00000507283.1:n.*232T>G
|
|
ENST00000683887.1:c.548T>G
|
ENSP00000506886.1:p.Leu183Arg
|
|
ENST00000684100.1:n.494T>G
|
|
|
ENST00000684126.1:n.558T>G
|
|
|
ENST00000684688.1:n.1125T>G
|
|
|
ENST00000204679.9:c.500T>G
MANE Select
|
ENSP00000204679.4:p.Leu167Arg
|
|
ENST00000204679.8:c.500T>G
|
ENSP00000204679.4:p.Leu167Arg
|
|
ENST00000527076.1:n.1516T>G
|
|
|
ENST00000527168.5:n.536T>G
|
|
|
ENST00000529957.5:n.599T>G
|
|
|
NM_032520.4:c.500T>G
|
NP_115909.1:p.Leu167Arg
|
|
XM_017023782.1:c.548T>G
|
XP_016879271.1:p.Leu183Arg
|
|
XM_017023783.1:c.140T>G
|
XP_016879272.1:p.Leu47Arg
|
|
NM_032520.5:c.500T>G
MANE Select
|
NP_115909.1:p.Leu167Arg
|
|