|
ENST00000434676.7:c.*551C>T
(DNM1L)
|
ENSP00000390090.2:n.*551C>T
|
|
|
ENST00000546757.6:c.*871C>T
(DNM1L)
|
ENSP00000448105.2:n.*871C>T
|
|
|
ENST00000547078.6:c.1224C>T
(DNM1L)
|
ENSP00000448802.2:p.Ala408=
|
|
|
ENST00000547719.2:n.2818C>T
(DNM1L)
|
|
|
|
ENST00000547932.6:c.*551C>T
(DNM1L)
|
ENSP00000515272.1:n.*551C>T
|
|
|
ENST00000548671.6:c.*732C>T
(DNM1L)
|
ENSP00000515271.1:n.*732C>T
|
|
|
ENST00000548750.6:c.1098C>T
(DNM1L)
|
ENSP00000447788.2:p.Ala366=
|
|
|
ENST00000549926.6:c.738C>T
(DNM1L)
|
ENSP00000515263.1:p.Ala246=
|
|
|
ENST00000550011.6:c.*1175C>T
(DNM1L)
|
ENSP00000515261.1:n.*1175C>T
|
|
|
ENST00000550093.6:n.1272C>T
(DNM1L)
|
|
|
|
ENST00000551076.6:c.*802C>T
(DNM1L)
|
ENSP00000515275.1:n.*802C>T
|
|
|
ENST00000551476.6:c.1134C>T
(DNM1L)
|
ENSP00000447845.2:p.Ala378=
|
|
|
ENST00000551643.6:c.*1016C>T
(DNM1L)
|
ENSP00000450401.1:n.*1016C>T
|
|
|
ENST00000703337.1:c.*982C>T
(DNM1L)
|
ENSP00000515262.1:n.*982C>T
|
|
|
ENST00000703338.1:c.738C>T
(DNM1L)
|
ENSP00000515264.1:p.Ala246=
|
|
|
ENST00000703360.1:c.*871C>T
(DNM1L)
|
ENSP00000515270.1:n.*871C>T
|
|
|
ENST00000703361.1:c.816C>T
(DNM1L)
|
ENSP00000515273.1:p.Ala272=
|
|
|
ENST00000703362.1:c.*551C>T
(DNM1L)
|
ENSP00000515274.1:n.*551C>T
|
|
|
ENST00000703363.1:n.2806C>T
(DNM1L)
|
|
|
|
ENST00000703364.1:n.2883C>T
(DNM1L)
|
|
|
|
ENST00000703365.1:c.*50C>T
(DNM1L)
|
ENSP00000515276.1:n.*50C>T
|
|
|
ENST00000703366.1:n.2245C>T
(DNM1L)
|
|
|
|
ENST00000703367.1:c.1185C>T
(DNM1L)
|
ENSP00000515277.1:p.Ala395=
|
|
|
ENST00000703368.1:c.*732C>T
(DNM1L)
|
ENSP00000515278.1:n.*732C>T
|
|
|
ENST00000703369.1:c.816C>T
(DNM1L)
|
ENSP00000515279.1:p.Ala272=
|
|
|
ENST00000703370.1:c.738C>T
(DNM1L)
|
ENSP00000515280.1:p.Ala246=
|
|
|
ENST00000703371.1:c.738C>T
(DNM1L)
|
ENSP00000515281.1:p.Ala246=
|
|
|
ENST00000703372.1:c.978C>T
(DNM1L)
|
ENSP00000515282.1:p.Ala326=
|
|
|
ENST00000549701.6:c.1185C>T
(DNM1L)
MANE Select
|
ENSP00000450399.1:p.Ala395=
|
|
|
ENST00000553257.6:c.1224C>T
(DNM1L)
MANE Plus Clinical
|
ENSP00000449089.1:p.Ala408=
|
|
|
ENST00000266481.10:c.1185C>T
(DNM1L)
|
ENSP00000266481.6:p.Ala395=
|
|
|
ENST00000358214.9:c.1224C>T
(DNM1L)
|
ENSP00000350948.5:p.Ala408=
|
|
|
ENST00000381000.8:c.1224C>T
(DNM1L)
|
ENSP00000370388.4:p.Ala408=
|
|
|
ENST00000413295.6:c.*434C>T
(DNM1L)
|
ENSP00000396030.2:n.*434C>T
|
|
|
ENST00000414834.6:c.576C>T
(DNM1L)
|
ENSP00000404160.2:p.Ala192=
|
|
|
ENST00000452533.6:c.1185C>T
(DNM1L)
|
ENSP00000415131.2:p.Ala395=
|
|
|
ENST00000546649.5:c.*427C>T
(DNM1L)
|
ENSP00000448936.1:n.*427C>T
|
|
|
ENST00000546757.5:c.1036C>T
(DNM1L)
|
ENSP00000448105.1:n.1036C>T
|
|
|
ENST00000547312.5:c.1185C>T
(DNM1L)
|
ENSP00000448610.1:p.Ala395=
|
|
|
ENST00000549701.5:c.1185C>T
(DNM1L)
|
ENSP00000450399.1:p.Ala395=
|
|
|
ENST00000551673.5:n.460-3600G>A
(YARS2)
|
|
|
|
ENST00000553257.5:c.1224C>T
(DNM1L)
|
ENSP00000449089.1:p.Ala408=
|
|
|
NM_001278463.1:c.1185C>T
(DNM1L)
|
NP_001265392.1:p.Ala395=
|
|
|
NM_001278464.1:c.1224C>T
(DNM1L)
|
NP_001265393.1:p.Ala408=
|
|
|
NM_001278465.1:c.1224C>T
(DNM1L)
|
NP_001265394.1:p.Ala408=
|
|
|
NM_001278466.1:c.576C>T
(DNM1L)
|
NP_001265395.1:p.Ala192=
|
|
|
NM_005690.4:c.1185C>T
(DNM1L)
|
NP_005681.2:p.Ala395=
|
|
|
NM_012062.4:c.1185C>T
(DNM1L)
|
NP_036192.2:p.Ala395=
|
|
|
NM_012063.3:c.1185C>T
(DNM1L)
|
NP_036193.2:p.Ala395=
|
|
|
XM_005253282.3:c.1224C>T
(DNM1L)
|
XP_005253339.1:p.Ala408=
|
|
|
XM_005253283.3:c.738C>T
(DNM1L)
|
XP_005253340.1:p.Ala246=
|
|
|
XM_011520543.1:c.1224C>T
(DNM1L)
|
XP_011518845.1:p.Ala408=
|
|
|
XM_011520544.1:c.528C>T
(DNM1L)
|
XP_011518846.1:p.Ala176=
|
|
|
XR_242891.3:n.1832+513G>A
(YARS2)
|
|
|
|
XR_242892.3:n.1650-5754G>A
(YARS2)
|
|
|
|
XR_429036.1:n.1707+513G>A
(YARS2)
|
|
|
|
XR_931297.1:n.1832+513G>A
(YARS2)
|
|
|
|
XR_931298.1:n.1707+513G>A
(YARS2)
|
|
|
|
XR_931299.1:n.1650-3600G>A
(YARS2)
|
|
|
|
NM_001330380.1:c.1224C>T
(DNM1L)
|
NP_001317309.1:p.Ala408=
|
|
|
XM_011520543.3:c.1224C>T
(DNM1L)
|
XP_011518845.1:p.Ala408=
|
|
|
XM_011520544.2:c.528C>T
(DNM1L)
|
XP_011518846.1:p.Ala176=
|
|
|
XM_017018663.2:c.528C>T
(DNM1L)
|
XP_016874152.1:p.Ala176=
|
|
|
XM_017018664.1:c.528C>T
(DNM1L)
|
XP_016874153.1:p.Ala176=
|
|
|
XM_017018665.1:c.528C>T
(DNM1L)
|
XP_016874154.1:p.Ala176=
|
|
|
XR_001748730.2:n.2272-5754G>A
(YARS2)
|
|
|
|
XR_002957331.1:n.2147-3600G>A
(YARS2)
|
|
|
|
XR_242892.5:n.2147-5754G>A
(YARS2)
|
|
|
|
NM_012062.5:c.1185C>T
(DNM1L)
MANE Select
|
NP_036192.2:p.Ala395=
|
|
|
NM_001278463.2:c.1185C>T
(DNM1L)
|
NP_001265392.1:p.Ala395=
|
|
|
NM_001278464.2:c.1224C>T
(DNM1L)
MANE Plus Clinical
|
NP_001265393.1:p.Ala408=
|
|
|
NM_001278465.2:c.1224C>T
(DNM1L)
|
NP_001265394.1:p.Ala408=
|
|
|
NM_001278466.2:c.576C>T
(DNM1L)
|
NP_001265395.1:p.Ala192=
|
|
|
NM_001330380.2:c.1224C>T
(DNM1L)
|
NP_001317309.1:p.Ala408=
|
|
|
NM_005690.5:c.1185C>T
(DNM1L)
|
NP_005681.2:p.Ala395=
|
|
|
NM_012063.4:c.1185C>T
(DNM1L)
|
NP_036193.2:p.Ala395=
|
|
