ENST00000634296.2:c.*411G>T
|
ENSP00000489512.2:n.*411G>T
|
|
ENST00000673864.2:c.*1322G>T
|
ENSP00000501045.2:n.*1322G>T
|
|
ENST00000674147.2:c.2092G>T
|
ENSP00000500964.2:p.Glu698Ter
|
|
ENST00000242839.10:c.2578G>T
MANE Select
|
ENSP00000242839.5:p.Glu860Ter
|
|
ENST00000344297.9:c.2092G>T
|
ENSP00000342559.5:p.Glu698Ter
|
|
ENST00000400366.6:c.2245G>T
|
ENSP00000383217.3:p.Glu749Ter
|
|
ENST00000448424.7:c.2326G>T
|
ENSP00000416738.3:p.Glu776Ter
|
|
ENST00000673772.1:c.2344G>T
|
ENSP00000501168.1:p.Glu782Ter
|
|
ENST00000674147.1:c.1648G>T
|
ENSP00000500964.1:p.Glu550Ter
|
|
ENST00000242839.8:c.2578G>T
|
ENSP00000242839.4:p.Glu860Ter
|
|
ENST00000344297.8:c.2092G>T
|
ENSP00000342559.5:p.Glu698Ter
|
|
ENST00000400366.5:c.2245G>T
|
ENSP00000383217.3:p.Glu749Ter
|
|
ENST00000400370.8:c.1288G>T
|
ENSP00000383221.3:p.Glu430Ter
|
|
ENST00000418097.7:c.2578G>T
|
ENSP00000393343.2:p.Glu860Ter
|
|
ENST00000448424.6:c.2344G>T
|
ENSP00000416738.2:p.Glu782Ter
|
|
ENST00000634296.1:c.539G>T
|
|
|
ENST00000634308.1:c.2344G>T
|
ENSP00000489234.1:p.Glu782Ter
|
|
ENST00000634620.1:n.3376G>T
|
|
|
ENST00000634810.1:n.1923G>T
|
|
|
ENST00000634844.1:c.2434G>T
|
ENSP00000489398.1:p.Glu812Ter
|
|
ENST00000635406.1:n.212-3681G>T
|
|
|
NM_000053.3:c.2578G>T
|
NP_000044.2:p.Glu860Ter
|
|
NM_001005918.2:c.2092G>T
|
NP_001005918.1:p.Glu698Ter
|
|
NM_001243182.1:c.2245G>T
|
NP_001230111.1:p.Glu749Ter
|
|
XM_005266423.2:c.2482G>T
|
XP_005266480.1:p.Glu828Ter
|
|
XM_005266424.3:c.2482G>T
|
XP_005266481.1:p.Glu828Ter
|
|
XM_005266427.2:c.2344G>T
|
XP_005266484.1:p.Glu782Ter
|
|
XM_005266428.1:c.2326G>T
|
XP_005266485.1:p.Glu776Ter
|
|
XM_005266430.3:c.2578G>T
|
XP_005266487.1:p.Glu860Ter
|
|
XM_005266431.2:c.2542G>T
|
XP_005266488.1:p.Glu848Ter
|
|
XM_005266432.2:c.2092G>T
|
XP_005266489.1:p.Glu698Ter
|
|
XM_006719837.2:c.2482G>T
|
XP_006719900.1:p.Glu828Ter
|
|
XM_006719838.1:c.394G>T
|
XP_006719901.1:p.Glu132Ter
|
|
XM_006719839.1:c.394G>T
|
XP_006719902.1:p.Glu132Ter
|
|
XM_011535117.1:c.2482G>T
|
XP_011533419.1:p.Glu828Ter
|
|
XM_011535118.1:c.2578G>T
|
XP_011533420.1:p.Glu860Ter
|
|
XM_011535119.1:c.2578G>T
|
XP_011533421.1:p.Glu860Ter
|
|
XM_011535120.1:c.2164G>T
|
XP_011533422.1:p.Glu722Ter
|
|
XM_011535121.1:c.2578G>T
|
XP_011533423.1:p.Glu860Ter
|
|
XM_011535122.1:c.1246G>T
|
XP_011533424.1:p.Glu416Ter
|
|
XR_941601.1:n.2797G>T
|
|
|
XR_941602.1:n.2797G>T
|
|
|
XR_941603.1:n.2797G>T
|
|
|
XR_941604.1:n.2797G>T
|
|
|
NM_001330578.1:c.2344G>T
|
NP_001317507.1:p.Glu782Ter
|
|
NM_001330579.1:c.2326G>T
|
NP_001317508.1:p.Glu776Ter
|
|
XM_005266424.4:c.2482G>T
|
XP_005266481.1:p.Glu828Ter
|
|
XM_005266430.4:c.2578G>T
|
XP_005266487.1:p.Glu860Ter
|
|
XM_005266431.4:c.2542G>T
|
XP_005266488.1:p.Glu848Ter
|
|
XM_006719837.3:c.2482G>T
|
XP_006719900.1:p.Glu828Ter
|
|
XM_011535117.3:c.2482G>T
|
XP_011533419.1:p.Glu828Ter
|
|
XM_017020627.1:c.2482G>T
|
XP_016876116.1:p.Glu828Ter
|
|
NM_000053.4:c.2578G>T
MANE Select
|
NP_000044.2:p.Glu860Ter
|
|
NM_001005918.3:c.2092G>T
|
NP_001005918.1:p.Glu698Ter
|
|
NM_001330579.2:c.2326G>T
|
NP_001317508.1:p.Glu776Ter
|
|
NM_001243182.2:c.2245G>T
|
NP_001230111.1:p.Glu749Ter
|
|
NM_001330578.2:c.2344G>T
|
NP_001317507.1:p.Glu782Ter
|
|