ENST00000682568.1:n.1762G=
|
|
|
ENST00000682617.1:c.1822G=
|
ENSP00000507912.1:p.Asp608=
|
|
ENST00000682826.1:c.*998G=
|
ENSP00000507274.1:n.*998G=
|
|
ENST00000682909.1:n.3724G=
|
|
|
ENST00000683277.1:n.3329G=
|
|
|
ENST00000683407.1:n.1692G=
|
|
|
ENST00000683962.1:c.*1378G=
|
ENSP00000506854.1:n.*1378G=
|
|
ENST00000311895.8:c.1684G=
MANE Select
|
ENSP00000310520.7:p.Asp562=
|
|
ENST00000311895.7:c.1684G=
|
ENSP00000310520.7:p.Asp562=
|
|
ENST00000389138.7:n.961G=
|
|
|
NM_005236.2:c.1684G= , LRG_463t1:c.1684G=
|
NP_005227.1:p.Asp562=
|
|
XM_011522424.1:c.1822G=
|
XP_011520726.1:p.Asp608=
|
|
XM_011522425.1:c.1141G=
|
XP_011520727.1:p.Asp381=
|
|
XM_011522426.1:c.895G=
|
XP_011520728.1:p.Asp299=
|
|
XM_011522427.1:c.334G=
|
XP_011520729.1:p.Asp112=
|
|
XR_932805.1:n.1843G=
|
|
|
XM_011522424.3:c.1822G=
|
XP_011520726.1:p.Asp608=
|
|
XM_017023043.2:c.895G=
|
XP_016878532.1:p.Asp299=
|
|
NM_005236.3:c.1684G=
MANE Select
|
NP_005227.1:p.Asp562=
|
|