ENST00000695850.1:n.384G>T
|
|
|
ENST00000695853.1:c.*267G>T
|
ENSP00000512218.1:n.*267G>T
|
|
ENST00000423902.7:c.7208G>T
MANE Select
|
ENSP00000392028.1:p.Arg2403Met
|
|
ENST00000423902.6:c.7208G>T
|
ENSP00000392028.1:p.Arg2403Met
|
|
ENST00000524602.5:c.1717-5741G>T
|
ENSP00000437061.1:n.1717-5741G>T
|
|
ENST00000529472.1:n.389G>T
|
|
|
NM_001316690.1:c.1717-5741G>T
|
NP_001303619.1:n.1717-5741G>T
|
|
NM_017780.3:c.7208G>T
|
NP_060250.2:p.Arg2403Met
|
|
XM_011517553.1:c.7298G>T
|
XP_011515855.1:p.Arg2433Met
|
|
XM_011517554.1:c.7298G>T
|
XP_011515856.1:p.Arg2433Met
|
|
XM_011517555.1:c.7295G>T
|
XP_011515857.1:p.Arg2432Met
|
|
XM_011517556.1:c.7298G>T
|
XP_011515858.1:p.Arg2433Met
|
|
XM_011517557.1:c.5285G>T
|
XP_011515859.1:p.Arg1762Met
|
|
XM_011517558.1:c.4835G>T
|
XP_011515860.1:p.Arg1612Met
|
|
XM_011517559.1:c.4043G>T
|
XP_011515861.1:p.Arg1348Met
|
|
XM_011517553.2:c.7298G>T
|
XP_011515855.1:p.Arg2433Met
|
|
XM_011517554.3:c.7298G>T
|
XP_011515856.1:p.Arg2433Met
|
|
XM_011517555.2:c.7295G>T
|
XP_011515857.1:p.Arg2432Met
|
|
XM_017013612.1:c.7298G>T
|
XP_016869101.1:p.Arg2433Met
|
|
XM_017013613.1:c.7205G>T
|
XP_016869102.1:p.Arg2402Met
|
|
NM_017780.4:c.7208G>T
MANE Select
|
NP_060250.2:p.Arg2403Met
|
|