ENST00000305188.13:c.1522A>G
MANE Select
|
ENSP00000306999.8:p.Ile508Val
|
|
ENST00000305188.12:c.1522A>G
|
ENSP00000306999.8:p.Ile508Val
|
|
ENST00000397418.4:c.466A>G
|
ENSP00000380563.2:p.Ile156Val
|
|
ENST00000518262.5:c.492A>G
|
|
|
ENST00000522378.5:c.*497A>G
|
ENSP00000428928.1:n.*497A>G
|
|
NM_001017420.2:c.1522A>G
|
NP_001017420.1:p.Ile508Val
|
|
XM_011544421.1:c.1522A>G
|
XP_011542723.1:p.Ile508Val
|
|
XM_011544422.1:c.1522A>G
|
XP_011542724.1:p.Ile508Val
|
|
XR_949378.1:n.1606A>G
|
|
|
XR_949379.1:n.1606A>G
|
|
|
XM_011544421.2:c.1522A>G
|
XP_011542723.1:p.Ile508Val
|
|
XM_011544422.2:c.1522A>G
|
XP_011542724.1:p.Ile508Val
|
|
XR_949378.3:n.1606A>G
|
|
|
NM_001017420.3:c.1522A>G
MANE Select
|
NP_001017420.1:p.Ile508Val
|
|