ENST00000342992.11:c.71033A>T
(TTN)
|
ENSP00000343764.6:p.Asp23678Val
|
|
ENST00000342175.11:c.52118A>T
(TTN)
|
ENSP00000340554.6:p.Asp17373Val
|
|
ENST00000359218.10:c.51917A>T
(TTN)
|
ENSP00000352154.5:p.Asp17306Val
|
|
ENST00000342175.10:c.52118A>T
(TTN)
|
ENSP00000340554.6:p.Asp17373Val
|
|
ENST00000342992.10:c.71033A>T
(TTN)
|
ENSP00000343764.6:p.Asp23678Val
|
|
ENST00000359218.9:c.51917A>T
(TTN)
|
ENSP00000352154.5:p.Asp17306Val
|
|
ENST00000460472.6:c.51542A>T
(TTN)
|
ENSP00000434586.1:p.Asp17181Val
|
|
ENST00000589042.5:c.78737A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp26246Val
|
|
ENST00000591111.5:c.73814A>T
(TTN)
|
ENSP00000465570.1:p.Asp24605Val
|
|
ENST00000615779.4:c.73814A>T
(TTN)
|
ENSP00000483597.1:p.Asp24605Val
|
|
NM_001256850.1:c.73814A>T
(TTN)
|
NP_001243779.1:p.Asp24605Val
|
|
NM_001267550.2:c.78737A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp26246Val
|
|
NM_003319.4:c.51542A>T
(TTN)
|
NP_003310.4:p.Asp17181Val
|
|
NM_133378.4:c.71033A>T
(TTN)
|
NP_596869.4:p.Asp23678Val
|
|
NM_133432.3:c.51917A>T
(TTN)
|
NP_597676.3:p.Asp17306Val
|
|
NM_133437.4:c.52118A>T
(TTN)
|
NP_597681.4:p.Asp17373Val
|
|
NR_038271.1:n.447-3905T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15177T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.77834A>T
(TTN)
|
XP_011510031.1:p.Asp25945Val
|
|
XM_011511730.1:c.51728A>T
(TTN)
|
XP_011510032.1:p.Asp17243Val
|
|
XM_011511731.1:c.51587A>T
(TTN)
|
XP_011510033.1:p.Asp17196Val
|
|
XM_017004819.1:c.77630A>T
(TTN)
|
XP_016860308.1:p.Asp25877Val
|
|
XM_017004820.1:c.73028A>T
(TTN)
|
XP_016860309.1:p.Asp24343Val
|
|
XM_017004821.1:c.73025A>T
(TTN)
|
XP_016860310.1:p.Asp24342Val
|
|
XM_017004822.1:c.70067A>T
(TTN)
|
XP_016860311.1:p.Asp23356Val
|
|
XM_017004823.1:c.51683A>T
(TTN)
|
XP_016860312.1:p.Asp17228Val
|
|
XM_024453094.1:c.73178A>T
(TTN)
|
XP_024308862.1:p.Asp24393Val
|
|
XM_024453095.1:c.73175A>T
(TTN)
|
XP_024308863.1:p.Asp24392Val
|
|
XM_024453096.1:c.72608A>T
(TTN)
|
XP_024308864.1:p.Asp24203Val
|
|
XM_024453097.1:c.69950A>T
(TTN)
|
XP_024308865.1:p.Asp23317Val
|
|
XM_024453098.1:c.69869A>T
(TTN)
|
XP_024308866.1:p.Asp23290Val
|
|
XM_024453099.1:c.51632A>T
(TTN)
|
XP_024308867.1:p.Asp17211Val
|
|
XM_024453100.1:c.41486A>T
(TTN)
|
XP_024308868.1:p.Asp13829Val
|
|