|
ENST00000435180.6:c.813A>G
|
ENSP00000391168.2:n.813A>G
|
|
|
ENST00000607071.6:c.*1321A>G
|
ENSP00000475855.1:n.*1321A>G
|
|
|
ENST00000642244.1:c.1511A>G
|
ENSP00000493554.1:p.His504Arg
|
|
|
ENST00000642903.1:c.1601A>G
|
ENSP00000493559.1:p.His534Arg
|
|
|
ENST00000644972.1:c.1601A>G
|
ENSP00000496451.1:p.His534Arg
|
|
|
ENST00000645077.1:c.*1222A>G
|
ENSP00000496113.1:n.*1222A>G
|
|
|
ENST00000645172.1:c.*1303A>G
|
ENSP00000495367.1:n.*1303A>G
|
|
|
ENST00000646190.1:n.2932A>G
|
|
|
|
ENST00000646208.1:c.1337A>G
|
ENSP00000493723.1:p.His446Arg
|
|
|
ENST00000646410.1:c.1472A>G
|
ENSP00000494205.1:p.His491Arg
|
|
|
ENST00000646562.1:c.*1435A>G
|
ENSP00000496087.1:n.*1435A>G
|
|
|
ENST00000647468.2:c.1601A>G
MANE Select
|
ENSP00000496731.1:p.His534Arg
|
|
|
ENST00000648111.1:c.*1289A>G
|
ENSP00000497275.1:n.*1289A>G
|
|
|
ENST00000367101.5:c.*49A>G
|
ENSP00000356068.1:n.*49A>G
|
|
|
ENST00000367104.7:c.1601A>G
|
ENSP00000356071.3:p.His534Arg
|
|
|
ENST00000435180.5:c.326A>G
|
ENSP00000391168.1:p.His109Arg
|
|
|
ENST00000606965.5:c.*162A>G
|
ENSP00000475808.1:n.*162A>G
|
|
|
ENST00000607071.5:c.*1535A>G
|
ENSP00000475855.1:n.*1535A>G
|
|
|
ENST00000607742.5:c.*2879A>G
|
ENSP00000475523.1:n.*2879A>G
|
|
|
NM_032861.3:c.1601A>G
|
NP_116250.3:p.His534Arg
|
|
|
NR_073096.1:n.1534A>G
|
|
|
|
XM_006715586.1:c.1391A>G
|
XP_006715649.1:p.His464Arg
|
|
|
XM_011536196.1:c.1580A>G
|
XP_011534498.1:p.His527Arg
|
|
|
XM_011536197.1:c.1487A>G
|
XP_011534499.1:p.His496Arg
|
|
|
XM_011536198.1:c.1391A>G
|
XP_011534500.1:p.His464Arg
|
|
|
XM_006715586.3:c.1391A>G
|
XP_006715649.1:p.His464Arg
|
|
|
XM_011536196.3:c.1580A>G
|
XP_011534498.1:p.His527Arg
|
|
|
XM_011536198.3:c.1391A>G
|
XP_011534500.1:p.His464Arg
|
|
|
XM_024446573.1:c.1601A>G
|
XP_024302341.1:p.His534Arg
|
|
|
XR_001743697.2:n.1632A>G
|
|
|
|
XR_942606.2:n.1683A>G
|
|
|
|
NM_032861.4:c.1601A>G
MANE Select
|
NP_116250.3:p.His534Arg
|
|
|
NR_073096.2:n.1516A>G
|
|
|
