ENST00000682263.1:n.3836T>A
|
|
|
ENST00000682317.1:c.*998T>A
|
ENSP00000508286.1:n.*998T>A
|
|
ENST00000683292.1:c.*832T>A
|
ENSP00000507503.1:n.*832T>A
|
|
ENST00000683293.1:n.3655T>A
|
|
|
ENST00000683744.1:c.*998T>A
|
ENSP00000506949.1:n.*998T>A
|
|
ENST00000684300.1:c.*998T>A
|
ENSP00000508407.1:n.*998T>A
|
|
ENST00000684400.1:n.2827T>A
|
|
|
ENST00000684436.1:n.2252T>A
|
|
|
ENST00000684510.1:n.2314T>A
|
|
|
ENST00000320356.7:c.1936T>A
MANE Select
|
ENSP00000320147.2:p.Tyr646Asn
|
|
ENST00000320356.6:c.1936T>A
|
ENSP00000320147.2:p.Tyr646Asn
|
|
ENST00000350995.6:c.1804T>A
|
ENSP00000223193.2:p.Tyr602Asn
|
|
ENST00000460911.5:c.1921T>A
|
ENSP00000419711.1:p.Tyr641Asn
|
|
ENST00000469631.1:n.188T>A
|
|
|
ENST00000476773.5:c.1768T>A
|
ENSP00000419050.1:p.Tyr590Asn
|
|
ENST00000478654.5:c.1768T>A
|
ENSP00000417062.1:p.Tyr590Asn
|
|
ENST00000483967.5:c.1894T>A
|
ENSP00000419856.1:p.Tyr632Asn
|
|
ENST00000492143.5:c.*1926T>A
|
ENSP00000417377.1:n.*1926T>A
|
|
NM_001203247.1:c.1921T>A
|
NP_001190176.1:p.Tyr641Asn
|
|
NM_001203248.1:c.1894T>A
|
NP_001190177.1:p.Tyr632Asn
|
|
NM_001203249.1:c.1768T>A
|
NP_001190178.1:p.Tyr590Asn
|
|
NM_004456.4:c.1936T>A , LRG_531t1:c.1936T>A
|
NP_004447.2:p.Tyr646Asn
|
|
NM_152998.2:c.1804T>A
|
NP_694543.1:p.Tyr602Asn
|
|
XM_005249962.3:c.1945T>A
|
XP_005250019.1:p.Tyr649Asn
|
|
XM_005249963.3:c.1918T>A
|
XP_005250020.1:p.Tyr640Asn
|
|
XM_005249964.3:c.1792T>A
|
XP_005250021.1:p.Tyr598Asn
|
|
XM_011515883.1:c.1960T>A
|
XP_011514185.1:p.Tyr654Asn
|
|
XM_011515884.1:c.1936T>A
|
XP_011514186.1:p.Tyr646Asn
|
|
XM_011515885.1:c.1933T>A
|
XP_011514187.1:p.Tyr645Asn
|
|
XM_011515886.1:c.1912T>A
|
XP_011514188.1:p.Tyr638Asn
|
|
XM_011515887.1:c.1909T>A
|
XP_011514189.1:p.Tyr637Asn
|
|
XM_011515888.1:c.1909T>A
|
XP_011514190.1:p.Tyr637Asn
|
|
XM_011515889.1:c.1870T>A
|
XP_011514191.1:p.Tyr624Asn
|
|
XM_011515890.1:c.1843T>A
|
XP_011514192.1:p.Tyr615Asn
|
|
XM_011515891.1:c.1837T>A
|
XP_011514193.1:p.Tyr613Asn
|
|
XM_011515892.1:c.1834T>A
|
XP_011514194.1:p.Tyr612Asn
|
|
XM_011515893.1:c.1828T>A
|
XP_011514195.1:p.Tyr610Asn
|
|
XM_011515894.1:c.1819T>A
|
XP_011514196.1:p.Tyr607Asn
|
|
XM_011515895.1:c.1816T>A
|
XP_011514197.1:p.Tyr606Asn
|
|
XM_011515896.1:c.1702T>A
|
XP_011514198.1:p.Tyr568Asn
|
|
XM_011515897.1:c.1609T>A
|
XP_011514199.1:p.Tyr537Asn
|
|
XM_011515898.1:c.1609T>A
|
XP_011514200.1:p.Tyr537Asn
|
|
XR_928101.1:n.515+6551A>T
|
|
|
XR_928102.1:n.722+6551A>T
|
|
|
XM_005249962.4:c.1945T>A
|
XP_005250019.1:p.Tyr649Asn
|
|
XM_005249963.4:c.1918T>A
|
XP_005250020.1:p.Tyr640Asn
|
|
XM_005249964.4:c.1792T>A
|
XP_005250021.1:p.Tyr598Asn
|
|
XM_011515883.2:c.1960T>A
|
XP_011514185.1:p.Tyr654Asn
|
|
XM_011515884.2:c.1936T>A
|
XP_011514186.1:p.Tyr646Asn
|
|
XM_011515885.2:c.1933T>A
|
XP_011514187.1:p.Tyr645Asn
|
|
XM_011515886.2:c.1912T>A
|
XP_011514188.1:p.Tyr638Asn
|
|
XM_011515887.3:c.1909T>A
|
XP_011514189.1:p.Tyr637Asn
|
|
XM_011515888.2:c.1909T>A
|
XP_011514190.1:p.Tyr637Asn
|
|
XM_011515889.2:c.1870T>A
|
XP_011514191.1:p.Tyr624Asn
|
|
XM_011515890.2:c.1843T>A
|
XP_011514192.1:p.Tyr615Asn
|
|
XM_011515891.3:c.1837T>A
|
XP_011514193.1:p.Tyr613Asn
|
|
XM_011515892.2:c.1834T>A
|
XP_011514194.1:p.Tyr612Asn
|
|
XM_011515893.2:c.1828T>A
|
XP_011514195.1:p.Tyr610Asn
|
|
XM_011515894.2:c.1819T>A
|
XP_011514196.1:p.Tyr607Asn
|
|
XM_011515895.2:c.1816T>A
|
XP_011514197.1:p.Tyr606Asn
|
|
XM_011515896.2:c.1702T>A
|
XP_011514198.1:p.Tyr568Asn
|
|
XM_011515897.2:c.1609T>A
|
XP_011514199.1:p.Tyr537Asn
|
|
XM_011515898.2:c.1609T>A
|
XP_011514200.1:p.Tyr537Asn
|
|
XM_017011817.2:c.1960T>A
|
XP_016867306.1:p.Tyr654Asn
|
|
XM_017011818.1:c.1897T>A
|
XP_016867307.1:p.Tyr633Asn
|
|
XM_017011819.1:c.1819T>A
|
XP_016867308.1:p.Tyr607Asn
|
|
XM_017011820.2:c.1792T>A
|
XP_016867309.1:p.Tyr598Asn
|
|
XM_017011821.1:c.1594T>A
|
XP_016867310.1:p.Tyr532Asn
|
|
XM_024446680.1:c.1822T>A
|
XP_024302448.1:p.Tyr608Asn
|
|
XR_001744581.1:n.4310T>A
|
|
|
XR_002956413.1:n.4966T>A
|
|
|
XR_002956414.1:n.5426T>A
|
|
|
NM_001203247.2:c.1921T>A
|
NP_001190176.1:p.Tyr641Asn
|
|
NM_001203248.2:c.1894T>A
|
NP_001190177.1:p.Tyr632Asn
|
|
NM_001203249.2:c.1768T>A
|
NP_001190178.1:p.Tyr590Asn
|
|
NM_004456.5:c.1936T>A
MANE Select
|
NP_004447.2:p.Tyr646Asn
|
|
NM_152998.3:c.1804T>A
|
NP_694543.1:p.Tyr602Asn
|
|