ENST00000342992.11:c.83457T>A
(TTN)
|
ENSP00000343764.6:p.Thr27819=
|
|
ENST00000342175.11:c.64542T>A
(TTN)
|
ENSP00000340554.6:p.Thr21514=
|
|
ENST00000359218.10:c.64341T>A
(TTN)
|
ENSP00000352154.5:p.Thr21447=
|
|
ENST00000342175.10:c.64542T>A
(TTN)
|
ENSP00000340554.6:p.Thr21514=
|
|
ENST00000342992.10:c.83457T>A
(TTN)
|
ENSP00000343764.6:p.Thr27819=
|
|
ENST00000359218.9:c.64341T>A
(TTN)
|
ENSP00000352154.5:p.Thr21447=
|
|
ENST00000460472.6:c.63966T>A
(TTN)
|
ENSP00000434586.1:p.Thr21322=
|
|
ENST00000589042.5:c.91161T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr30387=
|
|
ENST00000591111.5:c.86238T>A
(TTN)
|
ENSP00000465570.1:p.Thr28746=
|
|
ENST00000615779.4:c.86238T>A
(TTN)
|
ENSP00000483597.1:p.Thr28746=
|
|
NM_001256850.1:c.86238T>A
(TTN)
|
NP_001243779.1:p.Thr28746=
|
|
NM_001267550.2:c.91161T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr30387=
|
|
NM_003319.4:c.63966T>A
(TTN)
|
NP_003310.4:p.Thr21322=
|
|
NM_133378.4:c.83457T>A
(TTN)
|
NP_596869.4:p.Thr27819=
|
|
NM_133432.3:c.64341T>A
(TTN)
|
NP_597676.3:p.Thr21447=
|
|
NM_133437.4:c.64542T>A
(TTN)
|
NP_597681.4:p.Thr21514=
|
|
NR_038271.1:n.447-19561A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9378A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90258T>A
(TTN)
|
XP_011510031.1:p.Thr30086=
|
|
XM_011511730.1:c.64152T>A
(TTN)
|
XP_011510032.1:p.Thr21384=
|
|
XM_011511731.1:c.64011T>A
(TTN)
|
XP_011510033.1:p.Thr21337=
|
|
XM_017004819.1:c.90054T>A
(TTN)
|
XP_016860308.1:p.Thr30018=
|
|
XM_017004820.1:c.85452T>A
(TTN)
|
XP_016860309.1:p.Thr28484=
|
|
XM_017004821.1:c.85449T>A
(TTN)
|
XP_016860310.1:p.Thr28483=
|
|
XM_017004822.1:c.82491T>A
(TTN)
|
XP_016860311.1:p.Thr27497=
|
|
XM_017004823.1:c.64107T>A
(TTN)
|
XP_016860312.1:p.Thr21369=
|
|
XM_024453094.1:c.85602T>A
(TTN)
|
XP_024308862.1:p.Thr28534=
|
|
XM_024453095.1:c.85599T>A
(TTN)
|
XP_024308863.1:p.Thr28533=
|
|
XM_024453096.1:c.85032T>A
(TTN)
|
XP_024308864.1:p.Thr28344=
|
|
XM_024453097.1:c.82374T>A
(TTN)
|
XP_024308865.1:p.Thr27458=
|
|
XM_024453098.1:c.82293T>A
(TTN)
|
XP_024308866.1:p.Thr27431=
|
|
XM_024453099.1:c.64056T>A
(TTN)
|
XP_024308867.1:p.Thr21352=
|
|
XM_024453100.1:c.53910T>A
(TTN)
|
XP_024308868.1:p.Thr17970=
|
|