ENST00000342992.11:c.71043T>A
(TTN)
|
ENSP00000343764.6:p.Ala23681=
|
|
ENST00000342175.11:c.52128T>A
(TTN)
|
ENSP00000340554.6:p.Ala17376=
|
|
ENST00000359218.10:c.51927T>A
(TTN)
|
ENSP00000352154.5:p.Ala17309=
|
|
ENST00000342175.10:c.52128T>A
(TTN)
|
ENSP00000340554.6:p.Ala17376=
|
|
ENST00000342992.10:c.71043T>A
(TTN)
|
ENSP00000343764.6:p.Ala23681=
|
|
ENST00000359218.9:c.51927T>A
(TTN)
|
ENSP00000352154.5:p.Ala17309=
|
|
ENST00000460472.6:c.51552T>A
(TTN)
|
ENSP00000434586.1:p.Ala17184=
|
|
ENST00000589042.5:c.78747T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala26249=
|
|
ENST00000591111.5:c.73824T>A
(TTN)
|
ENSP00000465570.1:p.Ala24608=
|
|
ENST00000615779.4:c.73824T>A
(TTN)
|
ENSP00000483597.1:p.Ala24608=
|
|
NM_001256850.1:c.73824T>A
(TTN)
|
NP_001243779.1:p.Ala24608=
|
|
NM_001267550.2:c.78747T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala26249=
|
|
NM_003319.4:c.51552T>A
(TTN)
|
NP_003310.4:p.Ala17184=
|
|
NM_133378.4:c.71043T>A
(TTN)
|
NP_596869.4:p.Ala23681=
|
|
NM_133432.3:c.51927T>A
(TTN)
|
NP_597676.3:p.Ala17309=
|
|
NM_133437.4:c.52128T>A
(TTN)
|
NP_597681.4:p.Ala17376=
|
|
NR_038271.1:n.447-3915A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-15187A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.77844T>A
(TTN)
|
XP_011510031.1:p.Ala25948=
|
|
XM_011511730.1:c.51738T>A
(TTN)
|
XP_011510032.1:p.Ala17246=
|
|
XM_011511731.1:c.51597T>A
(TTN)
|
XP_011510033.1:p.Ala17199=
|
|
XM_017004819.1:c.77640T>A
(TTN)
|
XP_016860308.1:p.Ala25880=
|
|
XM_017004820.1:c.73038T>A
(TTN)
|
XP_016860309.1:p.Ala24346=
|
|
XM_017004821.1:c.73035T>A
(TTN)
|
XP_016860310.1:p.Ala24345=
|
|
XM_017004822.1:c.70077T>A
(TTN)
|
XP_016860311.1:p.Ala23359=
|
|
XM_017004823.1:c.51693T>A
(TTN)
|
XP_016860312.1:p.Ala17231=
|
|
XM_024453094.1:c.73188T>A
(TTN)
|
XP_024308862.1:p.Ala24396=
|
|
XM_024453095.1:c.73185T>A
(TTN)
|
XP_024308863.1:p.Ala24395=
|
|
XM_024453096.1:c.72618T>A
(TTN)
|
XP_024308864.1:p.Ala24206=
|
|
XM_024453097.1:c.69960T>A
(TTN)
|
XP_024308865.1:p.Ala23320=
|
|
XM_024453098.1:c.69879T>A
(TTN)
|
XP_024308866.1:p.Ala23293=
|
|
XM_024453099.1:c.51642T>A
(TTN)
|
XP_024308867.1:p.Ala17214=
|
|
XM_024453100.1:c.41496T>A
(TTN)
|
XP_024308868.1:p.Ala13832=
|
|