ENST00000342992.11:c.73916T>A
(TTN)
|
ENSP00000343764.6:p.Val24639Glu
|
|
ENST00000342175.11:c.55001T>A
(TTN)
|
ENSP00000340554.6:p.Val18334Glu
|
|
ENST00000359218.10:c.54800T>A
(TTN)
|
ENSP00000352154.5:p.Val18267Glu
|
|
ENST00000342175.10:c.55001T>A
(TTN)
|
ENSP00000340554.6:p.Val18334Glu
|
|
ENST00000342992.10:c.73916T>A
(TTN)
|
ENSP00000343764.6:p.Val24639Glu
|
|
ENST00000359218.9:c.54800T>A
(TTN)
|
ENSP00000352154.5:p.Val18267Glu
|
|
ENST00000460472.6:c.54425T>A
(TTN)
|
ENSP00000434586.1:p.Val18142Glu
|
|
ENST00000589042.5:c.81620T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val27207Glu
|
|
ENST00000591111.5:c.76697T>A
(TTN)
|
ENSP00000465570.1:p.Val25566Glu
|
|
ENST00000615779.4:c.76697T>A
(TTN)
|
ENSP00000483597.1:p.Val25566Glu
|
|
NM_001256850.1:c.76697T>A
(TTN)
|
NP_001243779.1:p.Val25566Glu
|
|
NM_001267550.2:c.81620T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val27207Glu
|
|
NM_003319.4:c.54425T>A
(TTN)
|
NP_003310.4:p.Val18142Glu
|
|
NM_133378.4:c.73916T>A
(TTN)
|
NP_596869.4:p.Val24639Glu
|
|
NM_133432.3:c.54800T>A
(TTN)
|
NP_597676.3:p.Val18267Glu
|
|
NM_133437.4:c.55001T>A
(TTN)
|
NP_597681.4:p.Val18334Glu
|
|
NR_038271.1:n.447-6788A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-18060A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.80717T>A
(TTN)
|
XP_011510031.1:p.Val26906Glu
|
|
XM_011511730.1:c.54611T>A
(TTN)
|
XP_011510032.1:p.Val18204Glu
|
|
XM_011511731.1:c.54470T>A
(TTN)
|
XP_011510033.1:p.Val18157Glu
|
|
XM_017004819.1:c.80513T>A
(TTN)
|
XP_016860308.1:p.Val26838Glu
|
|
XM_017004820.1:c.75911T>A
(TTN)
|
XP_016860309.1:p.Val25304Glu
|
|
XM_017004821.1:c.75908T>A
(TTN)
|
XP_016860310.1:p.Val25303Glu
|
|
XM_017004822.1:c.72950T>A
(TTN)
|
XP_016860311.1:p.Val24317Glu
|
|
XM_017004823.1:c.54566T>A
(TTN)
|
XP_016860312.1:p.Val18189Glu
|
|
XM_024453094.1:c.76061T>A
(TTN)
|
XP_024308862.1:p.Val25354Glu
|
|
XM_024453095.1:c.76058T>A
(TTN)
|
XP_024308863.1:p.Val25353Glu
|
|
XM_024453096.1:c.75491T>A
(TTN)
|
XP_024308864.1:p.Val25164Glu
|
|
XM_024453097.1:c.72833T>A
(TTN)
|
XP_024308865.1:p.Val24278Glu
|
|
XM_024453098.1:c.72752T>A
(TTN)
|
XP_024308866.1:p.Val24251Glu
|
|
XM_024453099.1:c.54515T>A
(TTN)
|
XP_024308867.1:p.Val18172Glu
|
|
XM_024453100.1:c.44369T>A
(TTN)
|
XP_024308868.1:p.Val14790Glu
|
|