ENST00000265113.9:c.*1122G>A
MANE Select
|
ENSP00000265113.4:n.*1122G>A
|
|
ENST00000381918.4:c.*1122G>A
|
ENSP00000371343.4:n.*1122G>A
|
|
ENST00000612708.5:c.*1122G>A
|
ENSP00000483657.1:n.*1122G>A
|
|
ENST00000613445.5:c.*1122G>A
|
ENSP00000477672.1:n.*1122G>A
|
|
ENST00000624112.2:n.5744G>A
|
|
|
ENST00000679784.1:c.*2663G>A
|
ENSP00000506030.1:n.*2663G>A
|
|
ENST00000679852.1:c.1561G>A
|
|
|
ENST00000679958.1:c.*1244G>A
|
ENSP00000505246.1:n.*1244G>A
|
|
ENST00000679983.1:c.*1122G>A
|
ENSP00000505238.1:n.*1122G>A
|
|
ENST00000679992.1:c.*1122G>A
|
ENSP00000506585.1:n.*1122G>A
|
|
ENST00000680048.1:c.*3244G>A
|
ENSP00000505296.1:n.*3244G>A
|
|
ENST00000680125.1:c.*1122G>A
|
ENSP00000506424.1:n.*1122G>A
|
|
ENST00000680232.1:c.*1122G>A
|
ENSP00000506207.1:n.*1122G>A
|
|
ENST00000680318.1:c.*1122G>A
|
ENSP00000505057.1:n.*1122G>A
|
|
ENST00000680568.1:n.1979G>A
|
|
|
ENST00000680655.1:c.*2463G>A
|
ENSP00000506436.1:n.*2463G>A
|
|
ENST00000680876.1:n.5932G>A
|
|
|
ENST00000680878.1:n.5797G>A
|
|
|
ENST00000681633.1:n.5559G>A
|
|
|
ENST00000681926.1:c.*1122G>A
|
ENSP00000505850.1:n.*1122G>A
|
|
ENST00000265113.8:c.*1122G>A
|
ENSP00000265113.4:n.*1122G>A
|
|
ENST00000381918.3:c.*1122G>A
|
ENSP00000371343.3:n.*1122G>A
|
|
ENST00000612708.4:c.*1122G>A
|
ENSP00000483657.1:n.*1122G>A
|
|
ENST00000613445.4:c.*1122G>A
|
ENSP00000477672.1:n.*1122G>A
|
|
NM_001166695.2:c.*1122G>A
|
NP_001160167.1:n.*1122G>A
|
|
NM_001289939.1:c.*1122G>A
|
NP_001276868.1:n.*1122G>A
|
|
NM_001289940.1:c.*1122G>A
|
NP_001276869.1:n.*1122G>A
|
|
NM_004172.4:c.*1122G>A
|
NP_004163.3:n.*1122G>A
|
|
XM_005248342.1:c.*1122G>A
|
XP_005248399.1:n.*1122G>A
|
|
XM_011514084.1:c.*1122G>A
|
XP_011512386.1:n.*1122G>A
|
|
XM_005248342.3:c.*1122G>A
|
XP_005248399.1:n.*1122G>A
|
|
XM_011514084.2:c.*1122G>A
|
XP_011512386.1:n.*1122G>A
|
|
XM_024446181.1:c.*1122G>A
|
XP_024301949.1:n.*1122G>A
|
|
XM_024446182.1:c.*1122G>A
|
XP_024301950.1:n.*1122G>A
|
|
NM_004172.5:c.*1122G>A
MANE Select
|
NP_004163.3:n.*1122G>A
|
|
NM_001166695.3:c.*1122G>A
|
NP_001160167.1:n.*1122G>A
|
|
NM_001289939.2:c.*1122G>A
|
NP_001276868.1:n.*1122G>A
|
|
NM_001289940.2:c.*1122G>A
|
NP_001276869.1:n.*1122G>A
|
|