ENST00000695850.1:n.1335G>C
|
|
|
ENST00000695852.1:n.266G>C
|
|
|
ENST00000695853.1:c.*1218G>C
|
ENSP00000512218.1:n.*1218G>C
|
|
ENST00000423902.7:c.8159G>C
MANE Select
|
ENSP00000392028.1:p.Arg2720Thr
|
|
ENST00000423902.6:c.8159G>C
|
ENSP00000392028.1:p.Arg2720Thr
|
|
ENST00000524602.5:c.2012G>C
|
ENSP00000437061.1:p.Arg671Thr
|
|
ENST00000528280.1:n.205G>C
|
|
|
ENST00000532149.1:n.581G>C
|
|
|
ENST00000618450.1:n.4195G>C
|
|
|
NM_001316690.1:c.2012G>C
|
NP_001303619.1:p.Arg671Thr
|
|
NM_017780.3:c.8159G>C
|
NP_060250.2:p.Arg2720Thr
|
|
XM_011517553.1:c.8249G>C
|
XP_011515855.1:p.Arg2750Thr
|
|
XM_011517554.1:c.8249G>C
|
XP_011515856.1:p.Arg2750Thr
|
|
XM_011517555.1:c.8246G>C
|
XP_011515857.1:p.Arg2749Thr
|
|
XM_011517556.1:c.8027G>C
|
XP_011515858.1:p.Arg2676Thr
|
|
XM_011517557.1:c.6236G>C
|
XP_011515859.1:p.Arg2079Thr
|
|
XM_011517558.1:c.5786G>C
|
XP_011515860.1:p.Arg1929Thr
|
|
XM_011517559.1:c.4994G>C
|
XP_011515861.1:p.Arg1665Thr
|
|
XM_011517553.2:c.8249G>C
|
XP_011515855.1:p.Arg2750Thr
|
|
XM_011517554.3:c.8249G>C
|
XP_011515856.1:p.Arg2750Thr
|
|
XM_011517555.2:c.8246G>C
|
XP_011515857.1:p.Arg2749Thr
|
|
XM_017013612.1:c.8249G>C
|
XP_016869101.1:p.Arg2750Thr
|
|
XM_017013613.1:c.8156G>C
|
XP_016869102.1:p.Arg2719Thr
|
|
NM_017780.4:c.8159G>C
MANE Select
|
NP_060250.2:p.Arg2720Thr
|
|