ENST00000695850.1:n.1443C>G
|
|
|
ENST00000695852.1:n.374C>G
|
|
|
ENST00000695853.1:c.*1326C>G
|
ENSP00000512218.1:n.*1326C>G
|
|
ENST00000423902.7:c.8267C>G
MANE Select
|
ENSP00000392028.1:p.Thr2756Arg
|
|
ENST00000423902.6:c.8267C>G
|
ENSP00000392028.1:p.Thr2756Arg
|
|
ENST00000524602.5:c.2120C>G
|
ENSP00000437061.1:p.Thr707Arg
|
|
ENST00000528280.1:n.313C>G
|
|
|
NM_001316690.1:c.2120C>G
|
NP_001303619.1:p.Thr707Arg
|
|
NM_017780.3:c.8267C>G
|
NP_060250.2:p.Thr2756Arg
|
|
XM_011517553.1:c.8357C>G
|
XP_011515855.1:p.Thr2786Arg
|
|
XM_011517554.1:c.8357C>G
|
XP_011515856.1:p.Thr2786Arg
|
|
XM_011517555.1:c.8354C>G
|
XP_011515857.1:p.Thr2785Arg
|
|
XM_011517556.1:c.8135C>G
|
XP_011515858.1:p.Thr2712Arg
|
|
XM_011517557.1:c.6344C>G
|
XP_011515859.1:p.Thr2115Arg
|
|
XM_011517558.1:c.5894C>G
|
XP_011515860.1:p.Thr1965Arg
|
|
XM_011517559.1:c.5102C>G
|
XP_011515861.1:p.Thr1701Arg
|
|
XM_011517553.2:c.8357C>G
|
XP_011515855.1:p.Thr2786Arg
|
|
XM_011517554.3:c.8357C>G
|
XP_011515856.1:p.Thr2786Arg
|
|
XM_011517555.2:c.8354C>G
|
XP_011515857.1:p.Thr2785Arg
|
|
XM_017013612.1:c.8357C>G
|
XP_016869101.1:p.Thr2786Arg
|
|
XM_017013613.1:c.8264C>G
|
XP_016869102.1:p.Thr2755Arg
|
|
NM_017780.4:c.8267C>G
MANE Select
|
NP_060250.2:p.Thr2756Arg
|
|