ENST00000342992.11:c.62342A>T
(TTN)
|
ENSP00000343764.6:p.Glu20781Val
|
|
ENST00000342175.11:c.43427A>T
(TTN)
|
ENSP00000340554.6:p.Glu14476Val
|
|
ENST00000359218.10:c.43226A>T
(TTN)
|
ENSP00000352154.5:p.Glu14409Val
|
|
ENST00000342175.10:c.43427A>T
(TTN)
|
ENSP00000340554.6:p.Glu14476Val
|
|
ENST00000342992.10:c.62342A>T
(TTN)
|
ENSP00000343764.6:p.Glu20781Val
|
|
ENST00000359218.9:c.43226A>T
(TTN)
|
ENSP00000352154.5:p.Glu14409Val
|
|
ENST00000460472.6:c.42851A>T
(TTN)
|
ENSP00000434586.1:p.Glu14284Val
|
|
ENST00000589042.5:c.70046A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu23349Val
|
|
ENST00000591111.5:c.65123A>T
(TTN)
|
ENSP00000465570.1:p.Glu21708Val
|
|
ENST00000615779.4:c.65123A>T
(TTN)
|
ENSP00000483597.1:p.Glu21708Val
|
|
NM_001256850.1:c.65123A>T
(TTN)
|
NP_001243779.1:p.Glu21708Val
|
|
NM_001267550.2:c.70046A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu23349Val
|
|
NM_003319.4:c.42851A>T
(TTN)
|
NP_003310.4:p.Glu14284Val
|
|
NM_133378.4:c.62342A>T
(TTN)
|
NP_596869.4:p.Glu20781Val
|
|
NM_133432.3:c.43226A>T
(TTN)
|
NP_597676.3:p.Glu14409Val
|
|
NM_133437.4:c.43427A>T
(TTN)
|
NP_597681.4:p.Glu14476Val
|
|
NR_038271.1:n.596+4637T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6486T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.69143A>T
(TTN)
|
XP_011510031.1:p.Glu23048Val
|
|
XM_011511730.1:c.43037A>T
(TTN)
|
XP_011510032.1:p.Glu14346Val
|
|
XM_011511731.1:c.42896A>T
(TTN)
|
XP_011510033.1:p.Glu14299Val
|
|
XM_017004819.1:c.68939A>T
(TTN)
|
XP_016860308.1:p.Glu22980Val
|
|
XM_017004820.1:c.64337A>T
(TTN)
|
XP_016860309.1:p.Glu21446Val
|
|
XM_017004821.1:c.64334A>T
(TTN)
|
XP_016860310.1:p.Glu21445Val
|
|
XM_017004822.1:c.61376A>T
(TTN)
|
XP_016860311.1:p.Glu20459Val
|
|
XM_017004823.1:c.42992A>T
(TTN)
|
XP_016860312.1:p.Glu14331Val
|
|
XM_024453094.1:c.64487A>T
(TTN)
|
XP_024308862.1:p.Glu21496Val
|
|
XM_024453095.1:c.64484A>T
(TTN)
|
XP_024308863.1:p.Glu21495Val
|
|
XM_024453096.1:c.63917A>T
(TTN)
|
XP_024308864.1:p.Glu21306Val
|
|
XM_024453097.1:c.61259A>T
(TTN)
|
XP_024308865.1:p.Glu20420Val
|
|
XM_024453098.1:c.61178A>T
(TTN)
|
XP_024308866.1:p.Glu20393Val
|
|
XM_024453099.1:c.42941A>T
(TTN)
|
XP_024308867.1:p.Glu14314Val
|
|
XM_024453100.1:c.32795A>T
(TTN)
|
XP_024308868.1:p.Glu10932Val
|
|