ENST00000682263.1:n.3950C>A
|
|
|
ENST00000682317.1:c.*1112C>A
|
ENSP00000508286.1:n.*1112C>A
|
|
ENST00000683292.1:c.*946C>A
|
ENSP00000507503.1:n.*946C>A
|
|
ENST00000683293.1:n.3769C>A
|
|
|
ENST00000683744.1:c.*1112C>A
|
ENSP00000506949.1:n.*1112C>A
|
|
ENST00000684300.1:c.*1112C>A
|
ENSP00000508407.1:n.*1112C>A
|
|
ENST00000684400.1:n.3883C>A
|
|
|
ENST00000684436.1:n.2366C>A
|
|
|
ENST00000684510.1:n.2428C>A
|
|
|
ENST00000320356.7:c.2050C>A
MANE Select
|
ENSP00000320147.2:p.Arg684Ser
|
|
ENST00000320356.6:c.2050C>A
|
ENSP00000320147.2:p.Arg684Ser
|
|
ENST00000350995.6:c.1918C>A
|
ENSP00000223193.2:p.Arg640Ser
|
|
ENST00000460911.5:c.2035C>A
|
ENSP00000419711.1:p.Arg679Ser
|
|
ENST00000476773.5:c.1882C>A
|
ENSP00000419050.1:p.Arg628Ser
|
|
ENST00000478654.5:c.1882C>A
|
ENSP00000417062.1:p.Arg628Ser
|
|
ENST00000483967.5:c.2008C>A
|
ENSP00000419856.1:p.Arg670Ser
|
|
ENST00000492143.5:c.*2040C>A
|
ENSP00000417377.1:n.*2040C>A
|
|
NM_001203247.1:c.2035C>A
|
NP_001190176.1:p.Arg679Ser
|
|
NM_001203248.1:c.2008C>A
|
NP_001190177.1:p.Arg670Ser
|
|
NM_001203249.1:c.1882C>A
|
NP_001190178.1:p.Arg628Ser
|
|
NM_004456.4:c.2050C>A , LRG_531t1:c.2050C>A
|
NP_004447.2:p.Arg684Ser
|
|
NM_152998.2:c.1918C>A
|
NP_694543.1:p.Arg640Ser
|
|
XM_005249962.3:c.2059C>A
|
XP_005250019.1:p.Arg687Ser
|
|
XM_005249963.3:c.2032C>A
|
XP_005250020.1:p.Arg678Ser
|
|
XM_005249964.3:c.1906C>A
|
XP_005250021.1:p.Arg636Ser
|
|
XM_011515883.1:c.2074C>A
|
XP_011514185.1:p.Arg692Ser
|
|
XM_011515884.1:c.2050C>A
|
XP_011514186.1:p.Arg684Ser
|
|
XM_011515885.1:c.2047C>A
|
XP_011514187.1:p.Arg683Ser
|
|
XM_011515886.1:c.2026C>A
|
XP_011514188.1:p.Arg676Ser
|
|
XM_011515887.1:c.2023C>A
|
XP_011514189.1:p.Arg675Ser
|
|
XM_011515888.1:c.2023C>A
|
XP_011514190.1:p.Arg675Ser
|
|
XM_011515889.1:c.1984C>A
|
XP_011514191.1:p.Arg662Ser
|
|
XM_011515890.1:c.1957C>A
|
XP_011514192.1:p.Arg653Ser
|
|
XM_011515891.1:c.1951C>A
|
XP_011514193.1:p.Arg651Ser
|
|
XM_011515892.1:c.1948C>A
|
XP_011514194.1:p.Arg650Ser
|
|
XM_011515893.1:c.1942C>A
|
XP_011514195.1:p.Arg648Ser
|
|
XM_011515894.1:c.1933C>A
|
XP_011514196.1:p.Arg645Ser
|
|
XM_011515895.1:c.1930C>A
|
XP_011514197.1:p.Arg644Ser
|
|
XM_011515896.1:c.1816C>A
|
XP_011514198.1:p.Arg606Ser
|
|
XM_011515897.1:c.1723C>A
|
XP_011514199.1:p.Arg575Ser
|
|
XM_011515898.1:c.1723C>A
|
XP_011514200.1:p.Arg575Ser
|
|
XR_928101.1:n.515+4285G>T
|
|
|
XR_928102.1:n.722+4285G>T
|
|
|
XM_005249962.4:c.2059C>A
|
XP_005250019.1:p.Arg687Ser
|
|
XM_005249963.4:c.2032C>A
|
XP_005250020.1:p.Arg678Ser
|
|
XM_005249964.4:c.1906C>A
|
XP_005250021.1:p.Arg636Ser
|
|
XM_011515883.2:c.2074C>A
|
XP_011514185.1:p.Arg692Ser
|
|
XM_011515884.2:c.2050C>A
|
XP_011514186.1:p.Arg684Ser
|
|
XM_011515885.2:c.2047C>A
|
XP_011514187.1:p.Arg683Ser
|
|
XM_011515886.2:c.2026C>A
|
XP_011514188.1:p.Arg676Ser
|
|
XM_011515887.3:c.2023C>A
|
XP_011514189.1:p.Arg675Ser
|
|
XM_011515888.2:c.2023C>A
|
XP_011514190.1:p.Arg675Ser
|
|
XM_011515889.2:c.1984C>A
|
XP_011514191.1:p.Arg662Ser
|
|
XM_011515890.2:c.1957C>A
|
XP_011514192.1:p.Arg653Ser
|
|
XM_011515891.3:c.1951C>A
|
XP_011514193.1:p.Arg651Ser
|
|
XM_011515892.2:c.1948C>A
|
XP_011514194.1:p.Arg650Ser
|
|
XM_011515893.2:c.1942C>A
|
XP_011514195.1:p.Arg648Ser
|
|
XM_011515894.2:c.1933C>A
|
XP_011514196.1:p.Arg645Ser
|
|
XM_011515895.2:c.1930C>A
|
XP_011514197.1:p.Arg644Ser
|
|
XM_011515896.2:c.1816C>A
|
XP_011514198.1:p.Arg606Ser
|
|
XM_011515897.2:c.1723C>A
|
XP_011514199.1:p.Arg575Ser
|
|
XM_011515898.2:c.1723C>A
|
XP_011514200.1:p.Arg575Ser
|
|
XM_017011817.2:c.2074C>A
|
XP_016867306.1:p.Arg692Ser
|
|
XM_017011818.1:c.2011C>A
|
XP_016867307.1:p.Arg671Ser
|
|
XM_017011819.1:c.1933C>A
|
XP_016867308.1:p.Arg645Ser
|
|
XM_017011820.2:c.1906C>A
|
XP_016867309.1:p.Arg636Ser
|
|
XM_017011821.1:c.1708C>A
|
XP_016867310.1:p.Arg570Ser
|
|
XM_024446680.1:c.1936C>A
|
XP_024302448.1:p.Arg646Ser
|
|
XR_001744581.1:n.4424C>A
|
|
|
XR_002956413.1:n.5080C>A
|
|
|
XR_002956414.1:n.5540C>A
|
|
|
NM_001203247.2:c.2035C>A
|
NP_001190176.1:p.Arg679Ser
|
|
NM_001203248.2:c.2008C>A
|
NP_001190177.1:p.Arg670Ser
|
|
NM_001203249.2:c.1882C>A
|
NP_001190178.1:p.Arg628Ser
|
|
NM_004456.5:c.2050C>A
MANE Select
|
NP_004447.2:p.Arg684Ser
|
|
NM_152998.3:c.1918C>A
|
NP_694543.1:p.Arg640Ser
|
|