ENST00000634296.2:c.*1240C>G
|
ENSP00000489512.2:n.*1240C>G
|
|
ENST00000673864.2:c.*2334C>G
|
ENSP00000501045.2:n.*2334C>G
|
|
ENST00000674147.2:c.2969C>G
|
ENSP00000500964.2:p.Ala990Gly
|
|
ENST00000242839.10:c.3590C>G
MANE Select
|
ENSP00000242839.5:p.Ala1197Gly
|
|
ENST00000344297.9:c.2969C>G
|
ENSP00000342559.5:p.Ala990Gly
|
|
ENST00000400366.6:c.3257C>G
|
ENSP00000383217.3:p.Ala1086Gly
|
|
ENST00000448424.7:c.3338C>G
|
ENSP00000416738.3:p.Ala1113Gly
|
|
ENST00000673696.1:n.831C>G
|
|
|
ENST00000673772.1:c.3356C>G
|
ENSP00000501168.1:p.Ala1119Gly
|
|
ENST00000673867.1:n.3729C>G
|
|
|
ENST00000673923.1:n.456C>G
|
|
|
ENST00000674147.1:c.2525C>G
|
ENSP00000500964.1:p.Ala842Gly
|
|
ENST00000242839.8:c.3590C>G
|
ENSP00000242839.4:p.Ala1197Gly
|
|
ENST00000344297.8:c.2969C>G
|
ENSP00000342559.5:p.Ala990Gly
|
|
ENST00000400366.5:c.3257C>G
|
ENSP00000383217.3:p.Ala1086Gly
|
|
ENST00000400370.8:c.2300C>G
|
ENSP00000383221.3:p.Ala767Gly
|
|
ENST00000418097.7:c.3395C>G
|
ENSP00000393343.2:p.Ala1132Gly
|
|
ENST00000448424.6:c.3356C>G
|
ENSP00000416738.2:p.Ala1119Gly
|
|
ENST00000634296.1:c.1368C>G
|
|
|
ENST00000634308.1:c.*691C>G
|
ENSP00000489234.1:n.*691C>G
|
|
ENST00000634620.1:n.4334C>G
|
|
|
ENST00000634810.1:n.2935C>G
|
|
|
ENST00000634844.1:c.3446C>G
|
ENSP00000489398.1:p.Ala1149Gly
|
|
NM_000053.3:c.3590C>G
|
NP_000044.2:p.Ala1197Gly
|
|
NM_001005918.2:c.2969C>G
|
NP_001005918.1:p.Ala990Gly
|
|
NM_001243182.1:c.3257C>G
|
NP_001230111.1:p.Ala1086Gly
|
|
XM_005266423.2:c.3494C>G
|
XP_005266480.1:p.Ala1165Gly
|
|
XM_005266424.3:c.3494C>G
|
XP_005266481.1:p.Ala1165Gly
|
|
XM_005266427.2:c.3356C>G
|
XP_005266484.1:p.Ala1119Gly
|
|
XM_005266428.1:c.3338C>G
|
XP_005266485.1:p.Ala1113Gly
|
|
XM_005266430.3:c.3590C>G
|
XP_005266487.1:p.Ala1197Gly
|
|
XM_005266431.2:c.3554C>G
|
XP_005266488.1:p.Ala1185Gly
|
|
XM_005266432.2:c.3104C>G
|
XP_005266489.1:p.Ala1035Gly
|
|
XM_006719837.2:c.3494C>G
|
XP_006719900.1:p.Ala1165Gly
|
|
XM_006719838.1:c.1406C>G
|
XP_006719901.1:p.Ala469Gly
|
|
XM_006719839.1:c.1223C>G
|
XP_006719902.1:p.Ala408Gly
|
|
XM_011535117.1:c.3494C>G
|
XP_011533419.1:p.Ala1165Gly
|
|
XM_011535118.1:c.3455C>G
|
XP_011533420.1:p.Ala1152Gly
|
|
XM_011535119.1:c.3407C>G
|
XP_011533421.1:p.Ala1136Gly
|
|
XM_011535120.1:c.3176C>G
|
XP_011533422.1:p.Ala1059Gly
|
|
XM_011535121.1:c.3077C>G
|
XP_011533423.1:p.Ala1026Gly
|
|
XM_011535122.1:c.2258C>G
|
XP_011533424.1:p.Ala753Gly
|
|
XR_941601.1:n.3809C>G
|
|
|
XR_941602.1:n.3809C>G
|
|
|
XR_941603.1:n.3809C>G
|
|
|
XR_941604.1:n.3809C>G
|
|
|
NM_001330578.1:c.3356C>G
|
NP_001317507.1:p.Ala1119Gly
|
|
NM_001330579.1:c.3338C>G
|
NP_001317508.1:p.Ala1113Gly
|
|
XM_005266424.4:c.3494C>G
|
XP_005266481.1:p.Ala1165Gly
|
|
XM_005266430.4:c.3590C>G
|
XP_005266487.1:p.Ala1197Gly
|
|
XM_005266431.4:c.3554C>G
|
XP_005266488.1:p.Ala1185Gly
|
|
XM_006719837.3:c.3494C>G
|
XP_006719900.1:p.Ala1165Gly
|
|
XM_011535117.3:c.3494C>G
|
XP_011533419.1:p.Ala1165Gly
|
|
XM_017020627.1:c.3494C>G
|
XP_016876116.1:p.Ala1165Gly
|
|
NM_000053.4:c.3590C>G
MANE Select
|
NP_000044.2:p.Ala1197Gly
|
|
NM_001005918.3:c.2969C>G
|
NP_001005918.1:p.Ala990Gly
|
|
NM_001330579.2:c.3338C>G
|
NP_001317508.1:p.Ala1113Gly
|
|
NM_001243182.2:c.3257C>G
|
NP_001230111.1:p.Ala1086Gly
|
|
NM_001330578.2:c.3356C>G
|
NP_001317507.1:p.Ala1119Gly
|
|