|
NM_000053.4:c.4016C>T
MANE Select
|
NP_000044.2:p.Ala1339Val
|
|
ENST00000242839.10:c.4016C>T
MANE Select
|
ENSP00000242839.5:p.Ala1339Val
|
|
NM_000053.3:c.4016C>T
|
NP_000044.2:p.Ala1339Val
|
|
NM_001005918.2:c.3395C>T
|
NP_001005918.1:p.Ala1132Val
|
|
NM_001005918.3:c.3395C>T
|
NP_001005918.1:p.Ala1132Val
|
|
NM_001243182.1:c.3683C>T
|
NP_001230111.1:p.Ala1228Val
|
|
NM_001243182.2:c.3683C>T
|
NP_001230111.1:p.Ala1228Val
|
|
NM_001330578.1:c.3782C>T
|
NP_001317507.1:p.Ala1261Val
|
|
NM_001330578.2:c.3782C>T
|
NP_001317507.1:p.Ala1261Val
|
|
NM_001330579.1:c.3764C>T
|
NP_001317508.1:p.Ala1255Val
|
|
NM_001330579.2:c.3764C>T
|
NP_001317508.1:p.Ala1255Val
|
|
ENST00000242839.8:c.4016C>T
|
ENSP00000242839.4:p.Ala1339Val
|
|
ENST00000344297.8:c.3395C>T
|
ENSP00000342559.5:p.Ala1132Val
|
|
ENST00000344297.9:c.3395C>T
|
ENSP00000342559.5:p.Ala1132Val
|
|
ENST00000400366.5:c.3683C>T
|
ENSP00000383217.3:p.Ala1228Val
|
|
ENST00000400366.6:c.3683C>T
|
ENSP00000383217.3:p.Ala1228Val
|
|
ENST00000400370.8:c.2726C>T
|
ENSP00000383221.3:p.Ala909Val
|
|
ENST00000418097.7:c.3821C>T
|
ENSP00000393343.2:p.Ala1274Val
|
|
ENST00000448424.6:c.3782C>T
|
ENSP00000416738.2:p.Ala1261Val
|
|
ENST00000448424.7:c.3764C>T
|
ENSP00000416738.3:p.Ala1255Val
|
|
ENST00000634296.1:c.1794C>T
|
|
|
ENST00000634296.2:c.*1666C>T
|
ENSP00000489512.2:n.*1666C>T
|
|
ENST00000634308.1:c.*1117C>T
|
ENSP00000489234.1:n.*1117C>T
|
|
ENST00000634620.1:n.4760C>T
|
|
|
ENST00000634810.1:n.3361C>T
|
|
|
ENST00000634844.1:c.3872C>T
|
ENSP00000489398.1:p.Ala1291Val
|
|
ENST00000673696.1:n.1339C>T
|
|
|
ENST00000673772.1:c.3782C>T
|
ENSP00000501168.1:p.Ala1261Val
|
|
ENST00000673864.2:c.*2760C>T
|
ENSP00000501045.2:n.*2760C>T
|
|
ENST00000673867.1:n.4155C>T
|
|
|
ENST00000673923.1:n.882C>T
|
|
|
ENST00000674147.1:c.2951C>T
|
ENSP00000500964.1:p.Ala984Val
|
|
ENST00000674147.2:c.3395C>T
|
ENSP00000500964.2:p.Ala1132Val
|
|
XM_005266423.2:c.3920C>T
|
XP_005266480.1:p.Ala1307Val
|
|
XM_005266424.3:c.3920C>T
|
XP_005266481.1:p.Ala1307Val
|
|
XM_005266424.4:c.3920C>T
|
XP_005266481.1:p.Ala1307Val
|
|
XM_005266427.2:c.3782C>T
|
XP_005266484.1:p.Ala1261Val
|
|
XM_005266428.1:c.3764C>T
|
XP_005266485.1:p.Ala1255Val
|
|
XM_005266430.3:c.4016C>T
|
XP_005266487.1:p.Ala1339Val
|
|
XM_005266430.4:c.4016C>T
|
XP_005266487.1:p.Ala1339Val
|
|
XM_005266431.2:c.3980C>T
|
XP_005266488.1:p.Ala1327Val
|
|
XM_005266431.4:c.3980C>T
|
XP_005266488.1:p.Ala1327Val
|
|
XM_005266432.2:c.3530C>T
|
XP_005266489.1:p.Ala1177Val
|
|
XM_006719837.2:c.3920C>T
|
XP_006719900.1:p.Ala1307Val
|
|
XM_006719837.3:c.3920C>T
|
XP_006719900.1:p.Ala1307Val
|
|
XM_006719838.1:c.1832C>T
|
XP_006719901.1:p.Ala611Val
|
|
XM_006719839.1:c.1649C>T
|
XP_006719902.1:p.Ala550Val
|
|
XM_011535117.1:c.3920C>T
|
XP_011533419.1:p.Ala1307Val
|
|
XM_011535117.3:c.3920C>T
|
XP_011533419.1:p.Ala1307Val
|
|
XM_011535118.1:c.3881C>T
|
XP_011533420.1:p.Ala1294Val
|
|
XM_011535119.1:c.3833C>T
|
XP_011533421.1:p.Ala1278Val
|
|
XM_011535120.1:c.3602C>T
|
XP_011533422.1:p.Ala1201Val
|
|
XM_011535121.1:c.3503C>T
|
XP_011533423.1:p.Ala1168Val
|
|
XM_011535122.1:c.2684C>T
|
XP_011533424.1:p.Ala895Val
|
|
XM_017020627.1:c.3920C>T
|
XP_016876116.1:p.Ala1307Val
|
|
XR_941601.1:n.4235C>T
|
|
|
XR_941602.1:n.4235C>T
|
|
|
XR_941603.1:n.4235C>T
|
|
|
XR_941604.1:n.4235C>T
|
|
