ENST00000342992.11:c.64551T>A
(TTN)
|
ENSP00000343764.6:p.Thr21517=
|
|
ENST00000342175.11:c.45636T>A
(TTN)
|
ENSP00000340554.6:p.Thr15212=
|
|
ENST00000359218.10:c.45435T>A
(TTN)
|
ENSP00000352154.5:p.Thr15145=
|
|
ENST00000342175.10:c.45636T>A
(TTN)
|
ENSP00000340554.6:p.Thr15212=
|
|
ENST00000342992.10:c.64551T>A
(TTN)
|
ENSP00000343764.6:p.Thr21517=
|
|
ENST00000359218.9:c.45435T>A
(TTN)
|
ENSP00000352154.5:p.Thr15145=
|
|
ENST00000460472.6:c.45060T>A
(TTN)
|
ENSP00000434586.1:p.Thr15020=
|
|
ENST00000589042.5:c.72255T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr24085=
|
|
ENST00000591111.5:c.67332T>A
(TTN)
|
ENSP00000465570.1:p.Thr22444=
|
|
ENST00000615779.4:c.67332T>A
(TTN)
|
ENSP00000483597.1:p.Thr22444=
|
|
NM_001256850.1:c.67332T>A
(TTN)
|
NP_001243779.1:p.Thr22444=
|
|
NM_001267550.2:c.72255T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr24085=
|
|
NM_003319.4:c.45060T>A
(TTN)
|
NP_003310.4:p.Thr15020=
|
|
NM_133378.4:c.64551T>A
(TTN)
|
NP_596869.4:p.Thr21517=
|
|
NM_133432.3:c.45435T>A
(TTN)
|
NP_597676.3:p.Thr15145=
|
|
NM_133437.4:c.45636T>A
(TTN)
|
NP_597681.4:p.Thr15212=
|
|
NR_038271.1:n.596+2428A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8695A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.71352T>A
(TTN)
|
XP_011510031.1:p.Thr23784=
|
|
XM_011511730.1:c.45246T>A
(TTN)
|
XP_011510032.1:p.Thr15082=
|
|
XM_011511731.1:c.45105T>A
(TTN)
|
XP_011510033.1:p.Thr15035=
|
|
XM_017004819.1:c.71148T>A
(TTN)
|
XP_016860308.1:p.Thr23716=
|
|
XM_017004820.1:c.66546T>A
(TTN)
|
XP_016860309.1:p.Thr22182=
|
|
XM_017004821.1:c.66543T>A
(TTN)
|
XP_016860310.1:p.Thr22181=
|
|
XM_017004822.1:c.63585T>A
(TTN)
|
XP_016860311.1:p.Thr21195=
|
|
XM_017004823.1:c.45201T>A
(TTN)
|
XP_016860312.1:p.Thr15067=
|
|
XM_024453094.1:c.66696T>A
(TTN)
|
XP_024308862.1:p.Thr22232=
|
|
XM_024453095.1:c.66693T>A
(TTN)
|
XP_024308863.1:p.Thr22231=
|
|
XM_024453096.1:c.66126T>A
(TTN)
|
XP_024308864.1:p.Thr22042=
|
|
XM_024453097.1:c.63468T>A
(TTN)
|
XP_024308865.1:p.Thr21156=
|
|
XM_024453098.1:c.63387T>A
(TTN)
|
XP_024308866.1:p.Thr21129=
|
|
XM_024453099.1:c.45150T>A
(TTN)
|
XP_024308867.1:p.Thr15050=
|
|
XM_024453100.1:c.35004T>A
(TTN)
|
XP_024308868.1:p.Thr11668=
|
|