|
ENST00000504687.7:c.1131T=
|
ENSP00000426535.3:p.His377=
|
|
|
ENST00000498722.3:n.921T=
|
|
|
|
ENST00000682650.1:c.1608+502T=
|
ENSP00000506904.1:n.1608+502T=
|
|
|
ENST00000683032.1:c.1689T=
|
ENSP00000506771.1:p.His563=
|
|
|
ENST00000683773.1:n.34T=
|
|
|
|
ENST00000684195.1:c.*37T=
|
ENSP00000508220.1:n.*37T=
|
|
|
ENST00000361308.9:c.1689T=
|
ENSP00000355292.6:p.His563=
|
|
|
ENST00000368300.9:c.1689T=
MANE Select
|
ENSP00000357283.4:p.His563=
|
|
|
ENST00000496738.6:n.2148T=
|
|
|
|
ENST00000674518.1:c.*1039T=
|
ENSP00000502261.1:n.*1039T=
|
|
|
ENST00000674600.1:c.*1488T=
|
ENSP00000501666.1:n.*1488T=
|
|
|
ENST00000674720.1:c.*251T=
|
ENSP00000502798.1:n.*251T=
|
|
|
ENST00000675431.1:n.1382T=
|
|
|
|
ENST00000675455.1:c.*1489T=
|
ENSP00000501795.1:n.*1489T=
|
|
|
ENST00000675667.1:c.1689T=
|
ENSP00000501803.1:p.His563=
|
|
|
ENST00000675874.1:c.*1160T=
|
ENSP00000501851.1:n.*1160T=
|
|
|
ENST00000675881.1:c.*700T=
|
ENSP00000501670.1:n.*700T=
|
|
|
ENST00000675939.1:c.1689T=
|
ENSP00000502256.1:p.His563=
|
|
|
ENST00000675989.1:n.2548T=
|
|
|
|
ENST00000676208.1:c.*792T=
|
ENSP00000502468.1:n.*792T=
|
|
|
ENST00000676283.1:n.2485T=
|
|
|
|
ENST00000676385.2:c.1608+502T=
|
ENSP00000502091.1:n.1608+502T=
|
|
|
ENST00000676434.1:c.*700T=
|
ENSP00000501648.1:n.*700T=
|
|
|
ENST00000677389.1:c.1689T=
MANE Plus Clinical
|
ENSP00000503633.1:p.His563=
|
|
|
ENST00000347559.6:c.1608+502T=
|
ENSP00000292304.3:n.1608+502T=
|
|
|
ENST00000361308.8:c.1434T=
|
ENSP00000355292.5:p.His478=
|
|
|
ENST00000368297.5:c.1446T=
|
ENSP00000357280.1:p.His482=
|
|
|
ENST00000368299.7:c.1689T=
|
ENSP00000357282.3:p.His563=
|
|
|
ENST00000368300.8:c.1689T=
|
ENSP00000357283.4:p.His563=
|
|
|
ENST00000368301.6:c.1689T=
|
ENSP00000357284.2:p.His563=
|
|
|
ENST00000448611.6:c.1353T=
|
ENSP00000395597.2:p.His451=
|
|
|
ENST00000473598.6:c.1392T=
|
ENSP00000421821.1:p.His464=
|
|
|
ENST00000496738.5:n.1158T=
|
|
|
|
ENST00000498722.2:n.921T=
|
|
|
|
ENST00000506981.1:n.273T=
|
|
|
|
ENST00000508500.1:c.486+502T=
|
ENSP00000424977.1:n.486+502T=
|
|
|
NM_001257374.2:c.1353T=
|
NP_001244303.1:p.His451=
|
|
|
NM_001282624.1:c.1446T=
|
NP_001269553.1:p.His482=
|
|
|
NM_001282625.1:c.1689T=
|
NP_001269554.1:p.His563=
|
|
|
NM_001282626.1:c.1689T=
|
NP_001269555.1:p.His563=
|
|
|
NM_005572.3:c.1689T= , LRG_254t1:c.1689T=
|
NP_005563.1:p.His563=
|
|
|
NM_170707.3:c.1689T=
|
NP_733821.1:p.His563=
|
|
|
NM_170708.3:c.1608+502T=
|
NP_733822.1:n.1608+502T=
|
|
|
XM_011509533.1:c.1353T=
|
XP_011507835.1:p.His451=
|
|
|
XM_011509534.1:c.1065T=
|
XP_011507836.1:p.His355=
|
|
|
XR_921781.1:n.1978T=
|
|
|
|
XM_011509534.2:c.1065T=
|
XP_011507836.1:p.His355=
|
|
|
XR_921781.2:n.1976T=
|
|
|
|
NM_170707.4:c.1689T=
MANE Select
|
NP_733821.1:p.His563=
|
|
|
NM_001257374.3:c.1353T=
|
NP_001244303.1:p.His451=
|
|
|
NM_001282626.2:c.1689T=
|
NP_001269555.1:p.His563=
|
|
|
NM_001282624.2:c.1446T=
|
NP_001269553.1:p.His482=
|
|
|
NM_001282625.2:c.1689T=
|
NP_001269554.1:p.His563=
|
|
|
NM_005572.4:c.1689T=
MANE Plus Clinical
|
NP_005563.1:p.His563=
|
|
|
NM_170708.4:c.1608+502T=
|
NP_733822.1:n.1608+502T=
|
|
