ENST00000682617.1:c.2244G>A
|
ENSP00000507912.1:p.Arg748=
|
|
ENST00000683962.1:c.*1800G>A
|
ENSP00000506854.1:n.*1800G>A
|
|
ENST00000311895.8:c.2106G>A
MANE Select
|
ENSP00000310520.7:p.Arg702=
|
|
ENST00000311895.7:c.2106G>A
|
ENSP00000310520.7:p.Arg702=
|
|
ENST00000389138.7:n.1383G>A
|
|
|
ENST00000462862.1:c.419G>A
|
ENSP00000461322.1:n.419G>A
|
|
NM_005236.2:c.2106G>A , LRG_463t1:c.2106G>A
|
NP_005227.1:p.Arg702=
|
|
XM_011522424.1:c.2244G>A
|
XP_011520726.1:p.Arg748=
|
|
XM_011522425.1:c.1563G>A
|
XP_011520727.1:p.Arg521=
|
|
XM_011522426.1:c.1317G>A
|
XP_011520728.1:p.Arg439=
|
|
XM_011522427.1:c.756G>A
|
XP_011520729.1:p.Arg252=
|
|
XR_932805.1:n.2265G>A
|
|
|
XM_011522424.3:c.2244G>A
|
XP_011520726.1:p.Arg748=
|
|
XM_017023043.2:c.1317G>A
|
XP_016878532.1:p.Arg439=
|
|
NM_005236.3:c.2106G>A
MANE Select
|
NP_005227.1:p.Arg702=
|
|