ENST00000634296.2:c.*894-1711T>G
|
ENSP00000489512.2:n.*894-1711T>G
|
|
ENST00000673864.2:c.*1831T>G
|
ENSP00000501045.2:n.*1831T>G
|
|
ENST00000674147.2:c.2466T>G
|
ENSP00000500964.2:p.Thr822=
|
|
ENST00000242839.10:c.3087T>G
MANE Select
|
ENSP00000242839.5:p.Thr1029=
|
|
ENST00000344297.9:c.2466T>G
|
ENSP00000342559.5:p.Thr822=
|
|
ENST00000400366.6:c.2754T>G
|
ENSP00000383217.3:p.Thr918=
|
|
ENST00000448424.7:c.2835T>G
|
ENSP00000416738.3:p.Thr945=
|
|
ENST00000673772.1:c.2853T>G
|
ENSP00000501168.1:p.Thr951=
|
|
ENST00000673867.1:n.3226T>G
|
|
|
ENST00000674126.1:n.3450T>G
|
|
|
ENST00000674147.1:c.2022T>G
|
ENSP00000500964.1:p.Thr674=
|
|
ENST00000242839.8:c.3087T>G
|
ENSP00000242839.4:p.Thr1029=
|
|
ENST00000344297.8:c.2466T>G
|
ENSP00000342559.5:p.Thr822=
|
|
ENST00000400366.5:c.2754T>G
|
ENSP00000383217.3:p.Thr918=
|
|
ENST00000400370.8:c.1797T>G
|
ENSP00000383221.3:p.Thr599=
|
|
ENST00000418097.7:c.2892T>G
|
ENSP00000393343.2:p.Thr964=
|
|
ENST00000448424.6:c.2853T>G
|
ENSP00000416738.2:p.Thr951=
|
|
ENST00000466629.1:n.307T>G
|
|
|
ENST00000634296.1:c.1022-1711T>G
|
|
|
ENST00000634308.1:c.*188T>G
|
ENSP00000489234.1:n.*188T>G
|
|
ENST00000634620.1:n.3831T>G
|
|
|
ENST00000634810.1:n.2432T>G
|
|
|
ENST00000634844.1:c.2943T>G
|
ENSP00000489398.1:p.Thr981=
|
|
ENST00000635406.1:n.433T>G
|
|
|
NM_000053.3:c.3087T>G
|
NP_000044.2:p.Thr1029=
|
|
NM_001005918.2:c.2466T>G
|
NP_001005918.1:p.Thr822=
|
|
NM_001243182.1:c.2754T>G
|
NP_001230111.1:p.Thr918=
|
|
XM_005266423.2:c.2991T>G
|
XP_005266480.1:p.Thr997=
|
|
XM_005266424.3:c.2991T>G
|
XP_005266481.1:p.Thr997=
|
|
XM_005266427.2:c.2853T>G
|
XP_005266484.1:p.Thr951=
|
|
XM_005266428.1:c.2835T>G
|
XP_005266485.1:p.Thr945=
|
|
XM_005266430.3:c.3087T>G
|
XP_005266487.1:p.Thr1029=
|
|
XM_005266431.2:c.3051T>G
|
XP_005266488.1:p.Thr1017=
|
|
XM_005266432.2:c.2601T>G
|
XP_005266489.1:p.Thr867=
|
|
XM_006719837.2:c.2991T>G
|
XP_006719900.1:p.Thr997=
|
|
XM_006719838.1:c.903T>G
|
XP_006719901.1:p.Thr301=
|
|
XM_006719839.1:c.877-1711T>G
|
XP_006719902.1:n.877-1711T>G
|
|
XM_011535117.1:c.2991T>G
|
XP_011533419.1:p.Thr997=
|
|
XM_011535118.1:c.2952T>G
|
XP_011533420.1:p.Thr984=
|
|
XM_011535119.1:c.3061-1711T>G
|
XP_011533421.1:n.3061-1711T>G
|
|
XM_011535120.1:c.2673T>G
|
XP_011533422.1:p.Thr891=
|
|
XM_011535121.1:c.2731-1711T>G
|
XP_011533423.1:n.2731-1711T>G
|
|
XM_011535122.1:c.1755T>G
|
XP_011533424.1:p.Thr585=
|
|
XR_941601.1:n.3306T>G
|
|
|
XR_941602.1:n.3306T>G
|
|
|
XR_941603.1:n.3306T>G
|
|
|
XR_941604.1:n.3306T>G
|
|
|
NM_001330578.1:c.2853T>G
|
NP_001317507.1:p.Thr951=
|
|
NM_001330579.1:c.2835T>G
|
NP_001317508.1:p.Thr945=
|
|
XM_005266424.4:c.2991T>G
|
XP_005266481.1:p.Thr997=
|
|
XM_005266430.4:c.3087T>G
|
XP_005266487.1:p.Thr1029=
|
|
XM_005266431.4:c.3051T>G
|
XP_005266488.1:p.Thr1017=
|
|
XM_006719837.3:c.2991T>G
|
XP_006719900.1:p.Thr997=
|
|
XM_011535117.3:c.2991T>G
|
XP_011533419.1:p.Thr997=
|
|
XM_017020627.1:c.2991T>G
|
XP_016876116.1:p.Thr997=
|
|
NM_000053.4:c.3087T>G
MANE Select
|
NP_000044.2:p.Thr1029=
|
|
NM_001005918.3:c.2466T>G
|
NP_001005918.1:p.Thr822=
|
|
NM_001330579.2:c.2835T>G
|
NP_001317508.1:p.Thr945=
|
|
NM_001243182.2:c.2754T>G
|
NP_001230111.1:p.Thr918=
|
|
NM_001330578.2:c.2853T>G
|
NP_001317507.1:p.Thr951=
|
|