|
NM_000053.4:c.3960G>T
MANE Select
|
NP_000044.2:p.Arg1320Ser
|
|
ENST00000242839.10:c.3960G>T
MANE Select
|
ENSP00000242839.5:p.Arg1320Ser
|
|
NM_000053.3:c.3960G>T
|
NP_000044.2:p.Arg1320Ser
|
|
NM_001005918.2:c.3339G>T
|
NP_001005918.1:p.Arg1113Ser
|
|
NM_001005918.3:c.3339G>T
|
NP_001005918.1:p.Arg1113Ser
|
|
NM_001243182.1:c.3627G>T
|
NP_001230111.1:p.Arg1209Ser
|
|
NM_001243182.2:c.3627G>T
|
NP_001230111.1:p.Arg1209Ser
|
|
NM_001330578.1:c.3726G>T
|
NP_001317507.1:p.Arg1242Ser
|
|
NM_001330578.2:c.3726G>T
|
NP_001317507.1:p.Arg1242Ser
|
|
NM_001330579.1:c.3708G>T
|
NP_001317508.1:p.Arg1236Ser
|
|
NM_001330579.2:c.3708G>T
|
NP_001317508.1:p.Arg1236Ser
|
|
ENST00000242839.8:c.3960G>T
|
ENSP00000242839.4:p.Arg1320Ser
|
|
ENST00000344297.8:c.3339G>T
|
ENSP00000342559.5:p.Arg1113Ser
|
|
ENST00000344297.9:c.3339G>T
|
ENSP00000342559.5:p.Arg1113Ser
|
|
ENST00000400366.5:c.3627G>T
|
ENSP00000383217.3:p.Arg1209Ser
|
|
ENST00000400366.6:c.3627G>T
|
ENSP00000383217.3:p.Arg1209Ser
|
|
ENST00000400370.8:c.2670G>T
|
ENSP00000383221.3:p.Arg890Ser
|
|
ENST00000418097.7:c.3765G>T
|
ENSP00000393343.2:p.Arg1255Ser
|
|
ENST00000448424.6:c.3726G>T
|
ENSP00000416738.2:p.Arg1242Ser
|
|
ENST00000448424.7:c.3708G>T
|
ENSP00000416738.3:p.Arg1236Ser
|
|
ENST00000634296.1:c.1738G>T
|
|
|
ENST00000634296.2:c.*1610G>T
|
ENSP00000489512.2:n.*1610G>T
|
|
ENST00000634308.1:c.*1061G>T
|
ENSP00000489234.1:n.*1061G>T
|
|
ENST00000634620.1:n.4704G>T
|
|
|
ENST00000634810.1:n.3305G>T
|
|
|
ENST00000634844.1:c.3816G>T
|
ENSP00000489398.1:p.Arg1272Ser
|
|
ENST00000673696.1:n.1283G>T
|
|
|
ENST00000673772.1:c.3726G>T
|
ENSP00000501168.1:p.Arg1242Ser
|
|
ENST00000673864.2:c.*2704G>T
|
ENSP00000501045.2:n.*2704G>T
|
|
ENST00000673867.1:n.4099G>T
|
|
|
ENST00000673923.1:n.826G>T
|
|
|
ENST00000674147.1:c.2895G>T
|
ENSP00000500964.1:p.Arg965Ser
|
|
ENST00000674147.2:c.3339G>T
|
ENSP00000500964.2:p.Arg1113Ser
|
|
XM_005266423.2:c.3864G>T
|
XP_005266480.1:p.Arg1288Ser
|
|
XM_005266424.3:c.3864G>T
|
XP_005266481.1:p.Arg1288Ser
|
|
XM_005266424.4:c.3864G>T
|
XP_005266481.1:p.Arg1288Ser
|
|
XM_005266427.2:c.3726G>T
|
XP_005266484.1:p.Arg1242Ser
|
|
XM_005266428.1:c.3708G>T
|
XP_005266485.1:p.Arg1236Ser
|
|
XM_005266430.3:c.3960G>T
|
XP_005266487.1:p.Arg1320Ser
|
|
XM_005266430.4:c.3960G>T
|
XP_005266487.1:p.Arg1320Ser
|
|
XM_005266431.2:c.3924G>T
|
XP_005266488.1:p.Arg1308Ser
|
|
XM_005266431.4:c.3924G>T
|
XP_005266488.1:p.Arg1308Ser
|
|
XM_005266432.2:c.3474G>T
|
XP_005266489.1:p.Arg1158Ser
|
|
XM_006719837.2:c.3864G>T
|
XP_006719900.1:p.Arg1288Ser
|
|
XM_006719837.3:c.3864G>T
|
XP_006719900.1:p.Arg1288Ser
|
|
XM_006719838.1:c.1776G>T
|
XP_006719901.1:p.Arg592Ser
|
|
XM_006719839.1:c.1593G>T
|
XP_006719902.1:p.Arg531Ser
|
|
XM_011535117.1:c.3864G>T
|
XP_011533419.1:p.Arg1288Ser
|
|
XM_011535117.3:c.3864G>T
|
XP_011533419.1:p.Arg1288Ser
|
|
XM_011535118.1:c.3825G>T
|
XP_011533420.1:p.Arg1275Ser
|
|
XM_011535119.1:c.3777G>T
|
XP_011533421.1:p.Arg1259Ser
|
|
XM_011535120.1:c.3546G>T
|
XP_011533422.1:p.Arg1182Ser
|
|
XM_011535121.1:c.3447G>T
|
XP_011533423.1:p.Arg1149Ser
|
|
XM_011535122.1:c.2628G>T
|
XP_011533424.1:p.Arg876Ser
|
|
XM_017020627.1:c.3864G>T
|
XP_016876116.1:p.Arg1288Ser
|
|
XR_941601.1:n.4179G>T
|
|
|
XR_941602.1:n.4179G>T
|
|
|
XR_941603.1:n.4179G>T
|
|
|
XR_941604.1:n.4179G>T
|
|
