|
ENST00000634296.2:c.1982C>G
|
ENSP00000489512.2:p.Thr661Arg
|
|
|
ENST00000673864.2:c.*901C>G
|
ENSP00000501045.2:n.*901C>G
|
|
|
ENST00000674147.2:c.1870-902C>G
|
ENSP00000500964.2:n.1870-902C>G
|
|
|
ENST00000242839.10:c.2157C>G
MANE Select
|
ENSP00000242839.5:p.Tyr719Ter
|
|
|
ENST00000344297.9:c.1870-902C>G
|
ENSP00000342559.5:n.1870-902C>G
|
|
|
ENST00000400366.6:c.1824C>G
|
ENSP00000383217.3:p.Tyr608Ter
|
|
|
ENST00000448424.7:c.1905C>G
|
ENSP00000416738.3:p.Tyr635Ter
|
|
|
ENST00000673772.1:c.2122-902C>G
|
ENSP00000501168.1:n.2122-902C>G
|
|
|
ENST00000674147.1:c.1426-902C>G
|
ENSP00000500964.1:n.1426-902C>G
|
|
|
ENST00000242839.8:c.2157C>G
|
ENSP00000242839.4:p.Tyr719Ter
|
|
|
ENST00000344297.8:c.1870-902C>G
|
ENSP00000342559.5:n.1870-902C>G
|
|
|
ENST00000400366.5:c.1824C>G
|
ENSP00000383217.3:p.Tyr608Ter
|
|
|
ENST00000400370.8:c.1286-8348C>G
|
ENSP00000383221.3:n.1286-8348C>G
|
|
|
ENST00000418097.7:c.2157C>G
|
ENSP00000393343.2:p.Tyr719Ter
|
|
|
ENST00000448424.6:c.2122-902C>G
|
ENSP00000416738.2:n.2122-902C>G
|
|
|
ENST00000482841.6:n.1700C>G
|
|
|
|
ENST00000634296.1:c.118C>G
|
|
|
|
ENST00000634308.1:c.2122-902C>G
|
ENSP00000489234.1:n.2122-902C>G
|
|
|
ENST00000634620.1:n.2252C>G
|
|
|
|
ENST00000634810.1:n.1502C>G
|
|
|
|
ENST00000634844.1:c.2122-109C>G
|
ENSP00000489398.1:n.2122-109C>G
|
|
|
ENST00000635406.1:n.212-12031C>G
|
|
|
|
NM_000053.3:c.2157C>G
|
NP_000044.2:p.Tyr719Ter
|
|
|
NM_001005918.2:c.1870-902C>G
|
NP_001005918.1:n.1870-902C>G
|
|
|
NM_001243182.1:c.1824C>G
|
NP_001230111.1:p.Tyr608Ter
|
|
|
XM_005266423.2:c.2061C>G
|
XP_005266480.1:p.Tyr687Ter
|
|
|
XM_005266424.3:c.2061C>G
|
XP_005266481.1:p.Tyr687Ter
|
|
|
XM_005266427.2:c.2122-902C>G
|
XP_005266484.1:n.2122-902C>G
|
|
|
XM_005266428.1:c.1905C>G
|
XP_005266485.1:p.Tyr635Ter
|
|
|
XM_005266430.3:c.2157C>G
|
XP_005266487.1:p.Tyr719Ter
|
|
|
XM_005266431.2:c.2121C>G
|
XP_005266488.1:p.Tyr707Ter
|
|
|
XM_005266432.2:c.1870-902C>G
|
XP_005266489.1:n.1870-902C>G
|
|
|
XM_006719837.2:c.2061C>G
|
XP_006719900.1:p.Tyr687Ter
|
|
|
XM_006719838.1:c.-28C>G
|
XP_006719901.1:n.-28C>G
|
|
|
XM_006719839.1:c.-28C>G
|
XP_006719902.1:n.-28C>G
|
|
|
XM_011535117.1:c.2061C>G
|
XP_011533419.1:p.Tyr687Ter
|
|
|
XM_011535118.1:c.2157C>G
|
XP_011533420.1:p.Tyr719Ter
|
|
|
XM_011535119.1:c.2157C>G
|
XP_011533421.1:p.Tyr719Ter
|
|
|
XM_011535120.1:c.1743C>G
|
XP_011533422.1:p.Tyr581Ter
|
|
|
XM_011535121.1:c.2157C>G
|
XP_011533423.1:p.Tyr719Ter
|
|
|
XM_011535122.1:c.825C>G
|
XP_011533424.1:p.Tyr275Ter
|
|
|
XR_941601.1:n.2376C>G
|
|
|
|
XR_941602.1:n.2376C>G
|
|
|
|
XR_941603.1:n.2376C>G
|
|
|
|
XR_941604.1:n.2376C>G
|
|
|
|
NM_001330578.1:c.2122-902C>G
|
NP_001317507.1:n.2122-902C>G
|
|
|
NM_001330579.1:c.1905C>G
|
NP_001317508.1:p.Tyr635Ter
|
|
|
XM_005266424.4:c.2061C>G
|
XP_005266481.1:p.Tyr687Ter
|
|
|
XM_005266430.4:c.2157C>G
|
XP_005266487.1:p.Tyr719Ter
|
|
|
XM_005266431.4:c.2121C>G
|
XP_005266488.1:p.Tyr707Ter
|
|
|
XM_006719837.3:c.2061C>G
|
XP_006719900.1:p.Tyr687Ter
|
|
|
XM_011535117.3:c.2061C>G
|
XP_011533419.1:p.Tyr687Ter
|
|
|
XM_017020627.1:c.2061C>G
|
XP_016876116.1:p.Tyr687Ter
|
|
|
NM_000053.4:c.2157C>G
MANE Select
|
NP_000044.2:p.Tyr719Ter
|
|
|
NM_001005918.3:c.1870-902C>G
|
NP_001005918.1:n.1870-902C>G
|
|
|
NM_001330579.2:c.1905C>G
|
NP_001317508.1:p.Tyr635Ter
|
|
|
NM_001243182.2:c.1824C>G
|
NP_001230111.1:p.Tyr608Ter
|
|
|
NM_001330578.2:c.2122-902C>G
|
NP_001317507.1:n.2122-902C>G
|
|
