|
ENST00000256578.8:c.1415T>G
|
ENSP00000256578.4:p.Met472Arg
|
|
|
ENST00000358729.9:c.1415T>G
|
ENSP00000351573.5:p.Met472Arg
|
|
|
ENST00000369840.7:c.1415T>G
|
ENSP00000358855.3:p.Met472Arg
|
|
|
ENST00000474459.6:n.2034T>G
|
|
|
|
ENST00000476688.3:c.1097T>G
|
ENSP00000437025.2:p.Met366Arg
|
|
|
ENST00000486282.7:n.2371T>G
|
|
|
|
ENST00000524975.2:n.1896T>G
|
|
|
|
ENST00000525415.2:n.1931T>G
|
|
|
|
ENST00000526301.6:n.1478T>G
|
|
|
|
ENST00000527846.7:n.1270T>G
|
|
|
|
ENST00000528667.7:c.1415T>G
MANE Select
|
ENSP00000436541.2:p.Met472Arg
|
|
|
ENST00000531203.6:c.1223T>G
|
ENSP00000431975.2:p.Met408Arg
|
|
|
ENST00000531734.6:c.1334T>G
|
ENSP00000433739.2:p.Met445Arg
|
|
|
ENST00000652975.2:c.*1167T>G
|
ENSP00000499620.2:n.*1167T>G
|
|
|
ENST00000654851.1:n.1257T>G
|
|
|
|
ENST00000655992.1:c.1223T>G
|
ENSP00000499740.1:p.Met408Arg
|
|
|
ENST00000659122.2:c.1407+155T>G
|
ENSP00000499621.2:n.1407+155T>G
|
|
|
ENST00000663749.1:c.*1162T>G
|
ENSP00000499739.1:n.*1162T>G
|
|
|
ENST00000667949.2:c.815T>G
|
ENSP00000499465.2:p.Met272Arg
|
|
|
ENST00000668421.1:c.*1356T>G
|
ENSP00000499362.1:n.*1356T>G
|
|
|
ENST00000679379.1:c.*1167T>G
|
ENSP00000505528.1:n.*1167T>G
|
|
|
ENST00000679593.1:c.1415T>G
|
ENSP00000505999.1:p.Met472Arg
|
|
|
ENST00000679880.1:n.1951T>G
|
|
|
|
ENST00000679892.1:c.*1183T>G
|
ENSP00000504882.1:n.*1183T>G
|
|
|
ENST00000679981.1:c.*1429T>G
|
ENSP00000506422.1:n.*1429T>G
|
|
|
ENST00000680132.1:c.*1365T>G
|
ENSP00000505950.1:n.*1365T>G
|
|
|
ENST00000680148.1:c.*1167T>G
|
ENSP00000505994.1:n.*1167T>G
|
|
|
ENST00000680170.1:n.2280T>G
|
|
|
|
ENST00000680192.1:n.2373T>G
|
|
|
|
ENST00000680519.1:n.1651T>G
|
|
|
|
ENST00000680531.1:c.*1162T>G
|
ENSP00000506332.1:n.*1162T>G
|
|
|
ENST00000680820.1:c.*1167T>G
|
ENSP00000505735.1:n.*1167T>G
|
|
|
ENST00000680832.1:c.*1515T>G
|
ENSP00000505774.1:n.*1515T>G
|
|
|
ENST00000680929.1:c.*1104T>G
|
ENSP00000504916.1:n.*1104T>G
|
|
|
ENST00000681108.1:c.*1245+155T>G
|
ENSP00000506701.1:n.*1245+155T>G
|
|
|
ENST00000681121.1:c.*525T>G
|
ENSP00000506466.1:n.*525T>G
|
|
|
ENST00000681132.1:c.*1181T>G
|
ENSP00000506195.1:n.*1181T>G
|
|
|
ENST00000681181.1:c.*1400T>G
|
ENSP00000506038.1:n.*1400T>G
|
|
|
ENST00000681218.1:c.*1688T>G
|
ENSP00000505976.1:n.*1688T>G
|
|
|
ENST00000681246.1:c.*1071T>G
|
ENSP00000505534.1:n.*1071T>G
|
|
|
ENST00000681496.1:c.*1688T>G
|
ENSP00000505948.1:n.*1688T>G
|
|
|
ENST00000681834.1:n.1754T>G
|
|
|
|
ENST00000681862.1:c.*1541T>G
|
ENSP00000505537.1:n.*1541T>G
|
|
|
ENST00000256578.7:c.1577T>G
|
ENSP00000256578.3:p.Met526Arg
|
|
|
ENST00000342115.8:c.1334T>G
|
ENSP00000345498.4:p.Met445Arg
|
|
|
ENST00000358729.8:c.1352T>G
|
ENSP00000351573.4:p.Met451Arg
|
|
|
ENST00000369840.6:c.1488T>G
|
|
|
|
ENST00000393688.7:c.1220T>G
|
ENSP00000377292.3:p.Met407Arg
|
|
|
ENST00000526301.5:n.1616T>G
|
|
|
|
ENST00000528454.5:c.1223T>G
|
ENSP00000437164.1:p.Met408Arg
|
|
|
ENST00000528667.5:c.1577T>G
|
ENSP00000436541.1:p.Met526Arg
|
|
|
ENST00000532851.1:n.125T>G
|
|
|
|
ENST00000533132.1:n.117T>G
|
|
|
|
NM_001257360.1:c.1577T>G
|
NP_001244289.1:p.Met526Arg
|
|
|
NM_001257361.1:c.1223T>G
|
NP_001244290.1:p.Met408Arg
|
|
|
NM_001308170.1:c.1352T>G
|
NP_001295099.1:p.Met451Arg
|
|
|
NM_004037.7:c.1577T>G
|
NP_004028.3:p.Met526Arg
|
|
|
NM_139156.3:c.1334T>G
|
NP_631895.1:p.Met445Arg
|
|
|
NM_203404.1:c.1220T>G
|
NP_981949.1:p.Met407Arg
|
|
|
XM_011541247.1:c.1790T>G
|
XP_011539549.1:p.Met597Arg
|
|
|
XM_011541248.1:c.1782+155T>G
|
XP_011539550.1:n.1782+155T>G
|
|
|
XR_946607.1:n.1813T>G
|
|
|
|
XM_024446431.1:c.1352T>G
|
XP_024302199.1:p.Met451Arg
|
|
|
XM_024446432.1:c.1430+155T>G
|
XP_024302200.1:n.1430+155T>G
|
|
|
XR_002956282.1:n.1988T>G
|
|
|
|
NM_001257360.2:c.1577T>G
|
NP_001244289.1:p.Met526Arg
|
|
|
NM_001368809.2:c.1415T>G
MANE Select
|
NP_001355738.1:p.Met472Arg
|
|
|
NM_004037.9:c.1415T>G
|
NP_004028.4:p.Met472Arg
|
|
|
NM_001257361.2:c.1223T>G
|
NP_001244290.1:p.Met408Arg
|
|
|
NM_139156.4:c.1334T>G
|
NP_631895.1:p.Met445Arg
|
|
