ENST00000682568.1:n.1868G>C
|
|
|
ENST00000682617.1:c.1928G>C
|
ENSP00000507912.1:p.Ser643Thr
|
|
ENST00000682826.1:c.*1104G>C
|
ENSP00000507274.1:n.*1104G>C
|
|
ENST00000682909.1:n.3830G>C
|
|
|
ENST00000683277.1:n.3435G>C
|
|
|
ENST00000683407.1:n.1798G>C
|
|
|
ENST00000683962.1:c.*1484G>C
|
ENSP00000506854.1:n.*1484G>C
|
|
ENST00000311895.8:c.1790G>C
MANE Select
|
ENSP00000310520.7:p.Ser597Thr
|
|
ENST00000311895.7:c.1790G>C
|
ENSP00000310520.7:p.Ser597Thr
|
|
ENST00000389138.7:n.1067G>C
|
|
|
NM_005236.2:c.1790G>C , LRG_463t1:c.1790G>C
|
NP_005227.1:p.Ser597Thr
|
|
XM_011522424.1:c.1928G>C
|
XP_011520726.1:p.Ser643Thr
|
|
XM_011522425.1:c.1247G>C
|
XP_011520727.1:p.Ser416Thr
|
|
XM_011522426.1:c.1001G>C
|
XP_011520728.1:p.Ser334Thr
|
|
XM_011522427.1:c.440G>C
|
XP_011520729.1:p.Ser147Thr
|
|
XR_932805.1:n.1949G>C
|
|
|
XM_011522424.3:c.1928G>C
|
XP_011520726.1:p.Ser643Thr
|
|
XM_017023043.2:c.1001G>C
|
XP_016878532.1:p.Ser334Thr
|
|
NM_005236.3:c.1790G>C
MANE Select
|
NP_005227.1:p.Ser597Thr
|
|