ENST00000634296.2:c.*1088G>T
|
ENSP00000489512.2:n.*1088G>T
|
|
ENST00000673864.2:c.*2182G>T
|
ENSP00000501045.2:n.*2182G>T
|
|
ENST00000674147.2:c.2817G>T
|
ENSP00000500964.2:p.Val939=
|
|
ENST00000242839.10:c.3438G>T
MANE Select
|
ENSP00000242839.5:p.Val1146=
|
|
ENST00000344297.9:c.2817G>T
|
ENSP00000342559.5:p.Val939=
|
|
ENST00000400366.6:c.3105G>T
|
ENSP00000383217.3:p.Val1035=
|
|
ENST00000448424.7:c.3186G>T
|
ENSP00000416738.3:p.Val1062=
|
|
ENST00000673772.1:c.3204G>T
|
ENSP00000501168.1:p.Val1068=
|
|
ENST00000673867.1:n.3577G>T
|
|
|
ENST00000674126.1:n.3801G>T
|
|
|
ENST00000674147.1:c.2373G>T
|
ENSP00000500964.1:p.Val791=
|
|
ENST00000242839.8:c.3438G>T
|
ENSP00000242839.4:p.Val1146=
|
|
ENST00000344297.8:c.2817G>T
|
ENSP00000342559.5:p.Val939=
|
|
ENST00000400366.5:c.3105G>T
|
ENSP00000383217.3:p.Val1035=
|
|
ENST00000400370.8:c.2148G>T
|
ENSP00000383221.3:p.Val716=
|
|
ENST00000418097.7:c.3243G>T
|
ENSP00000393343.2:p.Val1081=
|
|
ENST00000448424.6:c.3204G>T
|
ENSP00000416738.2:p.Val1068=
|
|
ENST00000634296.1:c.1216G>T
|
|
|
ENST00000634308.1:c.*539G>T
|
ENSP00000489234.1:n.*539G>T
|
|
ENST00000634620.1:n.4182G>T
|
|
|
ENST00000634810.1:n.2783G>T
|
|
|
ENST00000634844.1:c.3294G>T
|
ENSP00000489398.1:p.Val1098=
|
|
NM_000053.3:c.3438G>T
|
NP_000044.2:p.Val1146=
|
|
NM_001005918.2:c.2817G>T
|
NP_001005918.1:p.Val939=
|
|
NM_001243182.1:c.3105G>T
|
NP_001230111.1:p.Val1035=
|
|
XM_005266423.2:c.3342G>T
|
XP_005266480.1:p.Val1114=
|
|
XM_005266424.3:c.3342G>T
|
XP_005266481.1:p.Val1114=
|
|
XM_005266427.2:c.3204G>T
|
XP_005266484.1:p.Val1068=
|
|
XM_005266428.1:c.3186G>T
|
XP_005266485.1:p.Val1062=
|
|
XM_005266430.3:c.3438G>T
|
XP_005266487.1:p.Val1146=
|
|
XM_005266431.2:c.3402G>T
|
XP_005266488.1:p.Val1134=
|
|
XM_005266432.2:c.2952G>T
|
XP_005266489.1:p.Val984=
|
|
XM_006719837.2:c.3342G>T
|
XP_006719900.1:p.Val1114=
|
|
XM_006719838.1:c.1254G>T
|
XP_006719901.1:p.Val418=
|
|
XM_006719839.1:c.1071G>T
|
XP_006719902.1:p.Val357=
|
|
XM_011535117.1:c.3342G>T
|
XP_011533419.1:p.Val1114=
|
|
XM_011535118.1:c.3303G>T
|
XP_011533420.1:p.Val1101=
|
|
XM_011535119.1:c.3255G>T
|
XP_011533421.1:p.Val1085=
|
|
XM_011535120.1:c.3024G>T
|
XP_011533422.1:p.Val1008=
|
|
XM_011535121.1:c.2925G>T
|
XP_011533423.1:p.Val975=
|
|
XM_011535122.1:c.2106G>T
|
XP_011533424.1:p.Val702=
|
|
XR_941601.1:n.3657G>T
|
|
|
XR_941602.1:n.3657G>T
|
|
|
XR_941603.1:n.3657G>T
|
|
|
XR_941604.1:n.3657G>T
|
|
|
NM_001330578.1:c.3204G>T
|
NP_001317507.1:p.Val1068=
|
|
NM_001330579.1:c.3186G>T
|
NP_001317508.1:p.Val1062=
|
|
XM_005266424.4:c.3342G>T
|
XP_005266481.1:p.Val1114=
|
|
XM_005266430.4:c.3438G>T
|
XP_005266487.1:p.Val1146=
|
|
XM_005266431.4:c.3402G>T
|
XP_005266488.1:p.Val1134=
|
|
XM_006719837.3:c.3342G>T
|
XP_006719900.1:p.Val1114=
|
|
XM_011535117.3:c.3342G>T
|
XP_011533419.1:p.Val1114=
|
|
XM_017020627.1:c.3342G>T
|
XP_016876116.1:p.Val1114=
|
|
NM_000053.4:c.3438G>T
MANE Select
|
NP_000044.2:p.Val1146=
|
|
NM_001005918.3:c.2817G>T
|
NP_001005918.1:p.Val939=
|
|
NM_001330579.2:c.3186G>T
|
NP_001317508.1:p.Val1062=
|
|
NM_001243182.2:c.3105G>T
|
NP_001230111.1:p.Val1035=
|
|
NM_001330578.2:c.3204G>T
|
NP_001317507.1:p.Val1068=
|
|