ENST00000682263.1:n.3902T>C
|
|
|
ENST00000682317.1:c.*1064T>C
|
ENSP00000508286.1:n.*1064T>C
|
|
ENST00000683292.1:c.*898T>C
|
ENSP00000507503.1:n.*898T>C
|
|
ENST00000683293.1:n.3721T>C
|
|
|
ENST00000683744.1:c.*1064T>C
|
ENSP00000506949.1:n.*1064T>C
|
|
ENST00000684300.1:c.*1064T>C
|
ENSP00000508407.1:n.*1064T>C
|
|
ENST00000684400.1:n.2893T>C
|
|
|
ENST00000684436.1:n.2318T>C
|
|
|
ENST00000684510.1:n.2380T>C
|
|
|
ENST00000320356.7:c.2002T>C
MANE Select
|
ENSP00000320147.2:p.Cys668Arg
|
|
ENST00000320356.6:c.2002T>C
|
ENSP00000320147.2:p.Cys668Arg
|
|
ENST00000350995.6:c.1870T>C
|
ENSP00000223193.2:p.Cys624Arg
|
|
ENST00000460911.5:c.1987T>C
|
ENSP00000419711.1:p.Cys663Arg
|
|
ENST00000469631.1:n.254T>C
|
|
|
ENST00000476773.5:c.1834T>C
|
ENSP00000419050.1:p.Cys612Arg
|
|
ENST00000478654.5:c.1834T>C
|
ENSP00000417062.1:p.Cys612Arg
|
|
ENST00000483967.5:c.1960T>C
|
ENSP00000419856.1:p.Cys654Arg
|
|
ENST00000492143.5:c.*1992T>C
|
ENSP00000417377.1:n.*1992T>C
|
|
NM_001203247.1:c.1987T>C
|
NP_001190176.1:p.Cys663Arg
|
|
NM_001203248.1:c.1960T>C
|
NP_001190177.1:p.Cys654Arg
|
|
NM_001203249.1:c.1834T>C
|
NP_001190178.1:p.Cys612Arg
|
|
NM_004456.4:c.2002T>C , LRG_531t1:c.2002T>C
|
NP_004447.2:p.Cys668Arg
|
|
NM_152998.2:c.1870T>C
|
NP_694543.1:p.Cys624Arg
|
|
XM_005249962.3:c.2011T>C
|
XP_005250019.1:p.Cys671Arg
|
|
XM_005249963.3:c.1984T>C
|
XP_005250020.1:p.Cys662Arg
|
|
XM_005249964.3:c.1858T>C
|
XP_005250021.1:p.Cys620Arg
|
|
XM_011515883.1:c.2026T>C
|
XP_011514185.1:p.Cys676Arg
|
|
XM_011515884.1:c.2002T>C
|
XP_011514186.1:p.Cys668Arg
|
|
XM_011515885.1:c.1999T>C
|
XP_011514187.1:p.Cys667Arg
|
|
XM_011515886.1:c.1978T>C
|
XP_011514188.1:p.Cys660Arg
|
|
XM_011515887.1:c.1975T>C
|
XP_011514189.1:p.Cys659Arg
|
|
XM_011515888.1:c.1975T>C
|
XP_011514190.1:p.Cys659Arg
|
|
XM_011515889.1:c.1936T>C
|
XP_011514191.1:p.Cys646Arg
|
|
XM_011515890.1:c.1909T>C
|
XP_011514192.1:p.Cys637Arg
|
|
XM_011515891.1:c.1903T>C
|
XP_011514193.1:p.Cys635Arg
|
|
XM_011515892.1:c.1900T>C
|
XP_011514194.1:p.Cys634Arg
|
|
XM_011515893.1:c.1894T>C
|
XP_011514195.1:p.Cys632Arg
|
|
XM_011515894.1:c.1885T>C
|
XP_011514196.1:p.Cys629Arg
|
|
XM_011515895.1:c.1882T>C
|
XP_011514197.1:p.Cys628Arg
|
|
XM_011515896.1:c.1768T>C
|
XP_011514198.1:p.Cys590Arg
|
|
XM_011515897.1:c.1675T>C
|
XP_011514199.1:p.Cys559Arg
|
|
XM_011515898.1:c.1675T>C
|
XP_011514200.1:p.Cys559Arg
|
|
XR_928101.1:n.515+5275A>G
|
|
|
XR_928102.1:n.722+5275A>G
|
|
|
XM_005249962.4:c.2011T>C
|
XP_005250019.1:p.Cys671Arg
|
|
XM_005249963.4:c.1984T>C
|
XP_005250020.1:p.Cys662Arg
|
|
XM_005249964.4:c.1858T>C
|
XP_005250021.1:p.Cys620Arg
|
|
XM_011515883.2:c.2026T>C
|
XP_011514185.1:p.Cys676Arg
|
|
XM_011515884.2:c.2002T>C
|
XP_011514186.1:p.Cys668Arg
|
|
XM_011515885.2:c.1999T>C
|
XP_011514187.1:p.Cys667Arg
|
|
XM_011515886.2:c.1978T>C
|
XP_011514188.1:p.Cys660Arg
|
|
XM_011515887.3:c.1975T>C
|
XP_011514189.1:p.Cys659Arg
|
|
XM_011515888.2:c.1975T>C
|
XP_011514190.1:p.Cys659Arg
|
|
XM_011515889.2:c.1936T>C
|
XP_011514191.1:p.Cys646Arg
|
|
XM_011515890.2:c.1909T>C
|
XP_011514192.1:p.Cys637Arg
|
|
XM_011515891.3:c.1903T>C
|
XP_011514193.1:p.Cys635Arg
|
|
XM_011515892.2:c.1900T>C
|
XP_011514194.1:p.Cys634Arg
|
|
XM_011515893.2:c.1894T>C
|
XP_011514195.1:p.Cys632Arg
|
|
XM_011515894.2:c.1885T>C
|
XP_011514196.1:p.Cys629Arg
|
|
XM_011515895.2:c.1882T>C
|
XP_011514197.1:p.Cys628Arg
|
|
XM_011515896.2:c.1768T>C
|
XP_011514198.1:p.Cys590Arg
|
|
XM_011515897.2:c.1675T>C
|
XP_011514199.1:p.Cys559Arg
|
|
XM_011515898.2:c.1675T>C
|
XP_011514200.1:p.Cys559Arg
|
|
XM_017011817.2:c.2026T>C
|
XP_016867306.1:p.Cys676Arg
|
|
XM_017011818.1:c.1963T>C
|
XP_016867307.1:p.Cys655Arg
|
|
XM_017011819.1:c.1885T>C
|
XP_016867308.1:p.Cys629Arg
|
|
XM_017011820.2:c.1858T>C
|
XP_016867309.1:p.Cys620Arg
|
|
XM_017011821.1:c.1660T>C
|
XP_016867310.1:p.Cys554Arg
|
|
XM_024446680.1:c.1888T>C
|
XP_024302448.1:p.Cys630Arg
|
|
XR_001744581.1:n.4376T>C
|
|
|
XR_002956413.1:n.5032T>C
|
|
|
XR_002956414.1:n.5492T>C
|
|
|
NM_001203247.2:c.1987T>C
|
NP_001190176.1:p.Cys663Arg
|
|
NM_001203248.2:c.1960T>C
|
NP_001190177.1:p.Cys654Arg
|
|
NM_001203249.2:c.1834T>C
|
NP_001190178.1:p.Cys612Arg
|
|
NM_004456.5:c.2002T>C
MANE Select
|
NP_004447.2:p.Cys668Arg
|
|
NM_152998.3:c.1870T>C
|
NP_694543.1:p.Cys624Arg
|
|