ENST00000682568.1:n.1781G>C
|
|
|
ENST00000682617.1:c.1841G>C
|
ENSP00000507912.1:p.Arg614Thr
|
|
ENST00000682826.1:c.*1017G>C
|
ENSP00000507274.1:n.*1017G>C
|
|
ENST00000682909.1:n.3743G>C
|
|
|
ENST00000683277.1:n.3348G>C
|
|
|
ENST00000683407.1:n.1711G>C
|
|
|
ENST00000683962.1:c.*1397G>C
|
ENSP00000506854.1:n.*1397G>C
|
|
ENST00000311895.8:c.1703G>C
MANE Select
|
ENSP00000310520.7:p.Arg568Thr
|
|
ENST00000311895.7:c.1703G>C
|
ENSP00000310520.7:p.Arg568Thr
|
|
ENST00000389138.7:n.980G>C
|
|
|
NM_005236.2:c.1703G>C , LRG_463t1:c.1703G>C
|
NP_005227.1:p.Arg568Thr
|
|
XM_011522424.1:c.1841G>C
|
XP_011520726.1:p.Arg614Thr
|
|
XM_011522425.1:c.1160G>C
|
XP_011520727.1:p.Arg387Thr
|
|
XM_011522426.1:c.914G>C
|
XP_011520728.1:p.Arg305Thr
|
|
XM_011522427.1:c.353G>C
|
XP_011520729.1:p.Arg118Thr
|
|
XR_932805.1:n.1862G>C
|
|
|
XM_011522424.3:c.1841G>C
|
XP_011520726.1:p.Arg614Thr
|
|
XM_017023043.2:c.914G>C
|
XP_016878532.1:p.Arg305Thr
|
|
NM_005236.3:c.1703G>C
MANE Select
|
NP_005227.1:p.Arg568Thr
|
|