ENST00000682568.1:n.1760G>C
|
|
|
ENST00000682617.1:c.1820G>C
|
ENSP00000507912.1:p.Ser607Thr
|
|
ENST00000682826.1:c.*996G>C
|
ENSP00000507274.1:n.*996G>C
|
|
ENST00000682909.1:n.3722G>C
|
|
|
ENST00000683277.1:n.3327G>C
|
|
|
ENST00000683407.1:n.1690G>C
|
|
|
ENST00000683962.1:c.*1376G>C
|
ENSP00000506854.1:n.*1376G>C
|
|
ENST00000311895.8:c.1682G>C
MANE Select
|
ENSP00000310520.7:p.Ser561Thr
|
|
ENST00000311895.7:c.1682G>C
|
ENSP00000310520.7:p.Ser561Thr
|
|
ENST00000389138.7:n.959G>C
|
|
|
NM_005236.2:c.1682G>C , LRG_463t1:c.1682G>C
|
NP_005227.1:p.Ser561Thr
|
|
XM_011522424.1:c.1820G>C
|
XP_011520726.1:p.Ser607Thr
|
|
XM_011522425.1:c.1139G>C
|
XP_011520727.1:p.Ser380Thr
|
|
XM_011522426.1:c.893G>C
|
XP_011520728.1:p.Ser298Thr
|
|
XM_011522427.1:c.332G>C
|
XP_011520729.1:p.Ser111Thr
|
|
XR_932805.1:n.1841G>C
|
|
|
XM_011522424.3:c.1820G>C
|
XP_011520726.1:p.Ser607Thr
|
|
XM_017023043.2:c.893G>C
|
XP_016878532.1:p.Ser298Thr
|
|
NM_005236.3:c.1682G>C
MANE Select
|
NP_005227.1:p.Ser561Thr
|
|