ENST00000682568.1:n.1518C>G
|
|
|
ENST00000682617.1:c.1578C>G
|
ENSP00000507912.1:p.Thr526=
|
|
ENST00000682826.1:c.*754C>G
|
ENSP00000507274.1:n.*754C>G
|
|
ENST00000682909.1:n.3480C>G
|
|
|
ENST00000683277.1:n.3085C>G
|
|
|
ENST00000683407.1:n.1448C>G
|
|
|
ENST00000683962.1:c.*1134C>G
|
ENSP00000506854.1:n.*1134C>G
|
|
ENST00000311895.8:c.1440C>G
MANE Select
|
ENSP00000310520.7:p.Thr480=
|
|
ENST00000311895.7:c.1440C>G
|
ENSP00000310520.7:p.Thr480=
|
|
ENST00000389138.7:n.717C>G
|
|
|
ENST00000573018.1:n.508C>G
|
|
|
NM_005236.2:c.1440C>G , LRG_463t1:c.1440C>G
|
NP_005227.1:p.Thr480=
|
|
XM_011522424.1:c.1578C>G
|
XP_011520726.1:p.Thr526=
|
|
XM_011522425.1:c.897C>G
|
XP_011520727.1:p.Thr299=
|
|
XM_011522426.1:c.651C>G
|
XP_011520728.1:p.Thr217=
|
|
XM_011522427.1:c.90C>G
|
XP_011520729.1:p.Thr30=
|
|
XR_932805.1:n.1599C>G
|
|
|
XM_011522424.3:c.1578C>G
|
XP_011520726.1:p.Thr526=
|
|
XM_017023043.2:c.651C>G
|
XP_016878532.1:p.Thr217=
|
|
NM_005236.3:c.1440C>G
MANE Select
|
NP_005227.1:p.Thr480=
|
|