|
ENST00000504687.7:c.1140+11G=
|
ENSP00000426535.3:n.1140+11G=
|
|
|
ENST00000498722.3:n.941G=
|
|
|
|
ENST00000682650.1:c.1608+522G=
|
ENSP00000506904.1:n.1608+522G=
|
|
|
ENST00000683032.1:c.1698+11G=
|
ENSP00000506771.1:n.1698+11G=
|
|
|
ENST00000683773.1:n.43+11G=
|
|
|
|
ENST00000684195.1:c.*57G=
|
ENSP00000508220.1:n.*57G=
|
|
|
ENST00000361308.9:c.1698+11G=
|
ENSP00000355292.6:n.1698+11G=
|
|
|
ENST00000368300.9:c.1698+11G=
MANE Select
|
ENSP00000357283.4:n.1698+11G=
|
|
|
ENST00000496738.6:n.2168G=
|
|
|
|
ENST00000674518.1:c.*1048+11G=
|
ENSP00000502261.1:n.*1048+11G=
|
|
|
ENST00000674600.1:c.*1497+11G=
|
ENSP00000501666.1:n.*1497+11G=
|
|
|
ENST00000674720.1:c.*271G=
|
ENSP00000502798.1:n.*271G=
|
|
|
ENST00000675431.1:n.1402G=
|
|
|
|
ENST00000675455.1:c.*1498+11G=
|
ENSP00000501795.1:n.*1498+11G=
|
|
|
ENST00000675667.1:c.1698+11G=
|
ENSP00000501803.1:n.1698+11G=
|
|
|
ENST00000675874.1:c.*1169+11G=
|
ENSP00000501851.1:n.*1169+11G=
|
|
|
ENST00000675881.1:c.*709+11G=
|
ENSP00000501670.1:n.*709+11G=
|
|
|
ENST00000675939.1:c.1698+11G=
|
ENSP00000502256.1:n.1698+11G=
|
|
|
ENST00000675989.1:n.2568G=
|
|
|
|
ENST00000676208.1:c.*801+11G=
|
ENSP00000502468.1:n.*801+11G=
|
|
|
ENST00000676283.1:n.2505G=
|
|
|
|
ENST00000676385.2:c.1608+522G=
|
ENSP00000502091.1:n.1608+522G=
|
|
|
ENST00000676434.1:c.*720G=
|
ENSP00000501648.1:n.*720G=
|
|
|
ENST00000677389.1:c.1709G=
MANE Plus Clinical
|
ENSP00000503633.1:p.Ser570=
|
|
|
ENST00000347559.6:c.1608+522G=
|
ENSP00000292304.3:n.1608+522G=
|
|
|
ENST00000361308.8:c.1454G=
|
ENSP00000355292.5:p.Ser485=
|
|
|
ENST00000368297.5:c.1466G=
|
ENSP00000357280.1:p.Ser489=
|
|
|
ENST00000368299.7:c.1698+11G=
|
ENSP00000357282.3:n.1698+11G=
|
|
|
ENST00000368300.8:c.1698+11G=
|
ENSP00000357283.4:n.1698+11G=
|
|
|
ENST00000368301.6:c.1709G=
|
ENSP00000357284.2:p.Ser570=
|
|
|
ENST00000448611.6:c.1362+11G=
|
ENSP00000395597.2:n.1362+11G=
|
|
|
ENST00000473598.6:c.1401+11G=
|
ENSP00000421821.1:n.1401+11G=
|
|
|
ENST00000496738.5:n.1178G=
|
|
|
|
ENST00000498722.2:n.941G=
|
|
|
|
ENST00000506981.1:n.282+11G=
|
|
|
|
ENST00000508500.1:c.486+522G=
|
ENSP00000424977.1:n.486+522G=
|
|
|
NM_001257374.2:c.1362+11G=
|
NP_001244303.1:n.1362+11G=
|
|
|
NM_001282624.1:c.1466G=
|
NP_001269553.1:p.Ser489=
|
|
|
NM_001282625.1:c.1709G=
|
NP_001269554.1:p.Ser570=
|
|
|
NM_001282626.1:c.1698+11G=
|
NP_001269555.1:n.1698+11G=
|
|
|
NM_005572.3:c.1709G= , LRG_254t1:c.1709G=
|
NP_005563.1:p.Ser570=
|
|
|
NM_170707.3:c.1698+11G=
|
NP_733821.1:n.1698+11G=
|
|
|
NM_170708.3:c.1608+522G=
|
NP_733822.1:n.1608+522G=
|
|
|
XM_011509533.1:c.1362+11G=
|
XP_011507835.1:n.1362+11G=
|
|
|
XM_011509534.1:c.1074+11G=
|
XP_011507836.1:n.1074+11G=
|
|
|
XR_921781.1:n.1987+11G=
|
|
|
|
XM_011509534.2:c.1074+11G=
|
XP_011507836.1:n.1074+11G=
|
|
|
XR_921781.2:n.1985+11G=
|
|
|
|
NM_170707.4:c.1698+11G=
MANE Select
|
NP_733821.1:n.1698+11G=
|
|
|
NM_001257374.3:c.1362+11G=
|
NP_001244303.1:n.1362+11G=
|
|
|
NM_001282626.2:c.1698+11G=
|
NP_001269555.1:n.1698+11G=
|
|
|
NM_001282624.2:c.1466G=
|
NP_001269553.1:p.Ser489=
|
|
|
NM_001282625.2:c.1709G=
|
NP_001269554.1:p.Ser570=
|
|
|
NM_005572.4:c.1709G=
MANE Plus Clinical
|
NP_005563.1:p.Ser570=
|
|
|
NM_170708.4:c.1608+522G=
|
NP_733822.1:n.1608+522G=
|
|
