ENST00000682568.1:n.1496A>G
|
|
|
ENST00000682617.1:c.1556A>G
|
ENSP00000507912.1:p.Gln519Arg
|
|
ENST00000682826.1:c.*732A>G
|
ENSP00000507274.1:n.*732A>G
|
|
ENST00000682909.1:n.3458A>G
|
|
|
ENST00000683277.1:n.3063A>G
|
|
|
ENST00000683407.1:n.1426A>G
|
|
|
ENST00000683962.1:c.*1112A>G
|
ENSP00000506854.1:n.*1112A>G
|
|
ENST00000311895.8:c.1418A>G
MANE Select
|
ENSP00000310520.7:p.Gln473Arg
|
|
ENST00000311895.7:c.1418A>G
|
ENSP00000310520.7:p.Gln473Arg
|
|
ENST00000389138.7:n.695A>G
|
|
|
ENST00000573018.1:n.486A>G
|
|
|
NM_005236.2:c.1418A>G , LRG_463t1:c.1418A>G
|
NP_005227.1:p.Gln473Arg
|
|
XM_011522424.1:c.1556A>G
|
XP_011520726.1:p.Gln519Arg
|
|
XM_011522425.1:c.875A>G
|
XP_011520727.1:p.Gln292Arg
|
|
XM_011522426.1:c.629A>G
|
XP_011520728.1:p.Gln210Arg
|
|
XM_011522427.1:c.68A>G
|
XP_011520729.1:p.Gln23Arg
|
|
XR_932805.1:n.1577A>G
|
|
|
XM_011522424.3:c.1556A>G
|
XP_011520726.1:p.Gln519Arg
|
|
XM_017023043.2:c.629A>G
|
XP_016878532.1:p.Gln210Arg
|
|
NM_005236.3:c.1418A>G
MANE Select
|
NP_005227.1:p.Gln473Arg
|
|