ENST00000695850.1:n.1434T>C
|
|
|
ENST00000695852.1:n.365T>C
|
|
|
ENST00000695853.1:c.*1317T>C
|
ENSP00000512218.1:n.*1317T>C
|
|
ENST00000423902.7:c.8258T>C
MANE Select
|
ENSP00000392028.1:p.Met2753Thr
|
|
ENST00000423902.6:c.8258T>C
|
ENSP00000392028.1:p.Met2753Thr
|
|
ENST00000524602.5:c.2111T>C
|
ENSP00000437061.1:p.Met704Thr
|
|
ENST00000528280.1:n.304T>C
|
|
|
NM_001316690.1:c.2111T>C
|
NP_001303619.1:p.Met704Thr
|
|
NM_017780.3:c.8258T>C
|
NP_060250.2:p.Met2753Thr
|
|
XM_011517553.1:c.8348T>C
|
XP_011515855.1:p.Met2783Thr
|
|
XM_011517554.1:c.8348T>C
|
XP_011515856.1:p.Met2783Thr
|
|
XM_011517555.1:c.8345T>C
|
XP_011515857.1:p.Met2782Thr
|
|
XM_011517556.1:c.8126T>C
|
XP_011515858.1:p.Met2709Thr
|
|
XM_011517557.1:c.6335T>C
|
XP_011515859.1:p.Met2112Thr
|
|
XM_011517558.1:c.5885T>C
|
XP_011515860.1:p.Met1962Thr
|
|
XM_011517559.1:c.5093T>C
|
XP_011515861.1:p.Met1698Thr
|
|
XM_011517553.2:c.8348T>C
|
XP_011515855.1:p.Met2783Thr
|
|
XM_011517554.3:c.8348T>C
|
XP_011515856.1:p.Met2783Thr
|
|
XM_011517555.2:c.8345T>C
|
XP_011515857.1:p.Met2782Thr
|
|
XM_017013612.1:c.8348T>C
|
XP_016869101.1:p.Met2783Thr
|
|
XM_017013613.1:c.8255T>C
|
XP_016869102.1:p.Met2752Thr
|
|
NM_017780.4:c.8258T>C
MANE Select
|
NP_060250.2:p.Met2753Thr
|
|