ENST00000342992.11:c.88052T>A
(TTN)
|
ENSP00000343764.6:p.Val29351Glu
|
|
ENST00000342175.11:c.69137T>A
(TTN)
|
ENSP00000340554.6:p.Val23046Glu
|
|
ENST00000359218.10:c.68936T>A
(TTN)
|
ENSP00000352154.5:p.Val22979Glu
|
|
ENST00000342175.10:c.69137T>A
(TTN)
|
ENSP00000340554.6:p.Val23046Glu
|
|
ENST00000342992.10:c.88052T>A
(TTN)
|
ENSP00000343764.6:p.Val29351Glu
|
|
ENST00000359218.9:c.68936T>A
(TTN)
|
ENSP00000352154.5:p.Val22979Glu
|
|
ENST00000460472.6:c.68561T>A
(TTN)
|
ENSP00000434586.1:p.Val22854Glu
|
|
ENST00000589042.5:c.95756T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val31919Glu
|
|
ENST00000591111.5:c.90833T>A
(TTN)
|
ENSP00000465570.1:p.Val30278Glu
|
|
ENST00000615779.4:c.90833T>A
(TTN)
|
ENSP00000483597.1:p.Val30278Glu
|
|
NM_001256850.1:c.90833T>A
(TTN)
|
NP_001243779.1:p.Val30278Glu
|
|
NM_001267550.2:c.95756T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val31919Glu
|
|
NM_003319.4:c.68561T>A
(TTN)
|
NP_003310.4:p.Val22854Glu
|
|
NM_133378.4:c.88052T>A
(TTN)
|
NP_596869.4:p.Val29351Glu
|
|
NM_133432.3:c.68936T>A
(TTN)
|
NP_597676.3:p.Val22979Glu
|
|
NM_133437.4:c.69137T>A
(TTN)
|
NP_597681.4:p.Val23046Glu
|
|
NR_038271.1:n.446+20837A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2112A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.94853T>A
(TTN)
|
XP_011510031.1:p.Val31618Glu
|
|
XM_011511730.1:c.68747T>A
(TTN)
|
XP_011510032.1:p.Val22916Glu
|
|
XM_011511731.1:c.68606T>A
(TTN)
|
XP_011510033.1:p.Val22869Glu
|
|
XM_017004819.1:c.94649T>A
(TTN)
|
XP_016860308.1:p.Val31550Glu
|
|
XM_017004820.1:c.90047T>A
(TTN)
|
XP_016860309.1:p.Val30016Glu
|
|
XM_017004821.1:c.90044T>A
(TTN)
|
XP_016860310.1:p.Val30015Glu
|
|
XM_017004822.1:c.87086T>A
(TTN)
|
XP_016860311.1:p.Val29029Glu
|
|
XM_017004823.1:c.68702T>A
(TTN)
|
XP_016860312.1:p.Val22901Glu
|
|
XM_024453094.1:c.90197T>A
(TTN)
|
XP_024308862.1:p.Val30066Glu
|
|
XM_024453095.1:c.90194T>A
(TTN)
|
XP_024308863.1:p.Val30065Glu
|
|
XM_024453096.1:c.89627T>A
(TTN)
|
XP_024308864.1:p.Val29876Glu
|
|
XM_024453097.1:c.86969T>A
(TTN)
|
XP_024308865.1:p.Val28990Glu
|
|
XM_024453098.1:c.86888T>A
(TTN)
|
XP_024308866.1:p.Val28963Glu
|
|
XM_024453099.1:c.68651T>A
(TTN)
|
XP_024308867.1:p.Val22884Glu
|
|
XM_024453100.1:c.58505T>A
(TTN)
|
XP_024308868.1:p.Val19502Glu
|
|