ENST00000682568.1:n.1844G=
|
|
|
ENST00000682617.1:c.1904G=
|
ENSP00000507912.1:p.Arg635=
|
|
ENST00000682826.1:c.*1080G=
|
ENSP00000507274.1:n.*1080G=
|
|
ENST00000682909.1:n.3806G=
|
|
|
ENST00000683277.1:n.3411G=
|
|
|
ENST00000683407.1:n.1774G=
|
|
|
ENST00000683962.1:c.*1460G=
|
ENSP00000506854.1:n.*1460G=
|
|
ENST00000311895.8:c.1766G=
MANE Select
|
ENSP00000310520.7:p.Arg589=
|
|
ENST00000311895.7:c.1766G=
|
ENSP00000310520.7:p.Arg589=
|
|
ENST00000389138.7:n.1043G=
|
|
|
NM_005236.2:c.1766G= , LRG_463t1:c.1766G=
|
NP_005227.1:p.Arg589=
|
|
XM_011522424.1:c.1904G=
|
XP_011520726.1:p.Arg635=
|
|
XM_011522425.1:c.1223G=
|
XP_011520727.1:p.Arg408=
|
|
XM_011522426.1:c.977G=
|
XP_011520728.1:p.Arg326=
|
|
XM_011522427.1:c.416G=
|
XP_011520729.1:p.Arg139=
|
|
XR_932805.1:n.1925G=
|
|
|
XM_011522424.3:c.1904G=
|
XP_011520726.1:p.Arg635=
|
|
XM_017023043.2:c.977G=
|
XP_016878532.1:p.Arg326=
|
|
NM_005236.3:c.1766G=
MANE Select
|
NP_005227.1:p.Arg589=
|
|