ENST00000235329.10:c.816+372C>T
MANE Select
|
ENSP00000235329.5:n.816+372C>T
|
|
ENST00000674548.1:c.816+372C>T
|
ENSP00000502185.1:n.816+372C>T
|
|
ENST00000674658.1:c.471+372C>T
|
ENSP00000502334.1:n.471+372C>T
|
|
ENST00000674706.1:n.1627C>T
|
|
|
ENST00000674817.1:c.816+372C>T
|
ENSP00000502151.1:n.816+372C>T
|
|
ENST00000674910.1:c.816+372C>T
|
ENSP00000501716.1:n.816+372C>T
|
|
ENST00000675053.1:c.816+372C>T
|
ENSP00000501646.1:n.816+372C>T
|
|
ENST00000675113.1:c.816+372C>T
|
ENSP00000502623.1:n.816+372C>T
|
|
ENST00000675194.1:n.1241+372C>T
|
|
|
ENST00000675231.1:c.816+372C>T
|
ENSP00000502404.1:n.816+372C>T
|
|
ENST00000675298.1:c.816+372C>T
|
ENSP00000501839.1:n.816+372C>T
|
|
ENST00000675483.1:n.944+372C>T
|
|
|
ENST00000675512.1:c.*818+372C>T
|
ENSP00000502630.1:n.*818+372C>T
|
|
ENST00000675528.1:n.307+372C>T
|
|
|
ENST00000675817.1:c.816+372C>T
|
ENSP00000502422.1:n.816+372C>T
|
|
ENST00000675872.1:n.1176+372C>T
|
|
|
ENST00000675919.1:c.816+372C>T
|
ENSP00000501776.1:n.816+372C>T
|
|
ENST00000675959.1:n.1322+372C>T
|
|
|
ENST00000675987.1:c.816+372C>T
|
ENSP00000502145.1:n.816+372C>T
|
|
ENST00000676293.1:c.816+372C>T
|
ENSP00000502362.1:n.816+372C>T
|
|
ENST00000676426.1:c.600-1934C>T
|
ENSP00000502359.1:n.600-1934C>T
|
|
ENST00000235329.9:c.816+372C>T
|
ENSP00000235329.5:n.816+372C>T
|
|
ENST00000444836.5:c.816+372C>T
|
ENSP00000416338.1:n.816+372C>T
|
|
NM_001127660.1:c.816+372C>T
|
NP_001121132.1:n.816+372C>T
|
|
NM_014874.3:c.816+372C>T , LRG_255t1:c.816+372C>T
|
NP_055689.1:n.816+372C>T
|
|
XM_005263543.2:c.816+372C>T
|
XP_005263600.1:n.816+372C>T
|
|
XM_005263545.2:c.816+372C>T
|
XP_005263602.1:n.816+372C>T
|
|
XM_005263547.2:c.816+372C>T
|
XP_005263604.1:n.816+372C>T
|
|
XM_005263548.2:c.816+372C>T
|
XP_005263605.1:n.816+372C>T
|
|
XM_005263543.3:c.816+372C>T
|
XP_005263600.1:n.816+372C>T
|
|
XM_005263545.3:c.816+372C>T
|
XP_005263602.1:n.816+372C>T
|
|
XM_005263547.3:c.816+372C>T
|
XP_005263604.1:n.816+372C>T
|
|
XM_005263548.3:c.816+372C>T
|
XP_005263605.1:n.816+372C>T
|
|
XM_024451299.1:c.816+372C>T
|
XP_024307067.1:n.816+372C>T
|
|
NM_014874.4:c.816+372C>T
MANE Select
|
NP_055689.1:n.816+372C>T
|
|
NM_001127660.2:c.816+372C>T
|
NP_001121132.1:n.816+372C>T
|
|