ENST00000342992.11:c.98291T>A
(TTN)
|
ENSP00000343764.6:p.Phe32764Tyr
|
|
ENST00000342175.11:c.79376T>A
(TTN)
|
ENSP00000340554.6:p.Phe26459Tyr
|
|
ENST00000359218.10:c.79175T>A
(TTN)
|
ENSP00000352154.5:p.Phe26392Tyr
|
|
ENST00000342175.10:c.79376T>A
(TTN)
|
ENSP00000340554.6:p.Phe26459Tyr
|
|
ENST00000342992.10:c.98291T>A
(TTN)
|
ENSP00000343764.6:p.Phe32764Tyr
|
|
ENST00000359218.9:c.79175T>A
(TTN)
|
ENSP00000352154.5:p.Phe26392Tyr
|
|
ENST00000460472.6:c.78800T>A
(TTN)
|
ENSP00000434586.1:p.Phe26267Tyr
|
|
ENST00000589042.5:c.105995T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35332Tyr
|
|
ENST00000591111.5:c.101072T>A
(TTN)
|
ENSP00000465570.1:p.Phe33691Tyr
|
|
ENST00000615779.4:c.101072T>A
(TTN)
|
ENSP00000483597.1:p.Phe33691Tyr
|
|
NM_001256850.1:c.101072T>A
(TTN)
|
NP_001243779.1:p.Phe33691Tyr
|
|
NM_001267550.2:c.105995T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35332Tyr
|
|
NM_003319.4:c.78800T>A
(TTN)
|
NP_003310.4:p.Phe26267Tyr
|
|
NM_133378.4:c.98291T>A
(TTN)
|
NP_596869.4:p.Phe32764Tyr
|
|
NM_133432.3:c.79175T>A
(TTN)
|
NP_597676.3:p.Phe26392Tyr
|
|
NM_133437.4:c.79376T>A
(TTN)
|
NP_597681.4:p.Phe26459Tyr
|
|
NR_038271.1:n.446+6984A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5112A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105092T>A
(TTN)
|
XP_011510031.1:p.Phe35031Tyr
|
|
XM_011511730.1:c.78986T>A
(TTN)
|
XP_011510032.1:p.Phe26329Tyr
|
|
XM_011511731.1:c.78845T>A
(TTN)
|
XP_011510033.1:p.Phe26282Tyr
|
|
XM_017004819.1:c.104888T>A
(TTN)
|
XP_016860308.1:p.Phe34963Tyr
|
|
XM_017004820.1:c.100286T>A
(TTN)
|
XP_016860309.1:p.Phe33429Tyr
|
|
XM_017004821.1:c.100283T>A
(TTN)
|
XP_016860310.1:p.Phe33428Tyr
|
|
XM_017004822.1:c.97325T>A
(TTN)
|
XP_016860311.1:p.Phe32442Tyr
|
|
XM_017004823.1:c.78941T>A
(TTN)
|
XP_016860312.1:p.Phe26314Tyr
|
|
XM_024453094.1:c.100436T>A
(TTN)
|
XP_024308862.1:p.Phe33479Tyr
|
|
XM_024453095.1:c.100433T>A
(TTN)
|
XP_024308863.1:p.Phe33478Tyr
|
|
XM_024453096.1:c.99866T>A
(TTN)
|
XP_024308864.1:p.Phe33289Tyr
|
|
XM_024453097.1:c.97208T>A
(TTN)
|
XP_024308865.1:p.Phe32403Tyr
|
|
XM_024453098.1:c.97127T>A
(TTN)
|
XP_024308866.1:p.Phe32376Tyr
|
|
XM_024453099.1:c.78890T>A
(TTN)
|
XP_024308867.1:p.Phe26297Tyr
|
|
XM_024453100.1:c.68744T>A
(TTN)
|
XP_024308868.1:p.Phe22915Tyr
|
|