ENST00000342992.11:c.88208C>T
(TTN)
|
ENSP00000343764.6:p.Thr29403Ile
|
|
ENST00000342175.11:c.69293C>T
(TTN)
|
ENSP00000340554.6:p.Thr23098Ile
|
|
ENST00000359218.10:c.69092C>T
(TTN)
|
ENSP00000352154.5:p.Thr23031Ile
|
|
ENST00000342175.10:c.69293C>T
(TTN)
|
ENSP00000340554.6:p.Thr23098Ile
|
|
ENST00000342992.10:c.88208C>T
(TTN)
|
ENSP00000343764.6:p.Thr29403Ile
|
|
ENST00000359218.9:c.69092C>T
(TTN)
|
ENSP00000352154.5:p.Thr23031Ile
|
|
ENST00000460472.6:c.68717C>T
(TTN)
|
ENSP00000434586.1:p.Thr22906Ile
|
|
ENST00000589042.5:c.95912C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31971Ile
|
|
ENST00000591111.5:c.90989C>T
(TTN)
|
ENSP00000465570.1:p.Thr30330Ile
|
|
ENST00000615779.4:c.90989C>T
(TTN)
|
ENSP00000483597.1:p.Thr30330Ile
|
|
NM_001256850.1:c.90989C>T
(TTN)
|
NP_001243779.1:p.Thr30330Ile
|
|
NM_001267550.2:c.95912C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31971Ile
|
|
NM_003319.4:c.68717C>T
(TTN)
|
NP_003310.4:p.Thr22906Ile
|
|
NM_133378.4:c.88208C>T
(TTN)
|
NP_596869.4:p.Thr29403Ile
|
|
NM_133432.3:c.69092C>T
(TTN)
|
NP_597676.3:p.Thr23031Ile
|
|
NM_133437.4:c.69293C>T
(TTN)
|
NP_597681.4:p.Thr23098Ile
|
|
NR_038271.1:n.446+20681G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1956G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95009C>T
(TTN)
|
XP_011510031.1:p.Thr31670Ile
|
|
XM_011511730.1:c.68903C>T
(TTN)
|
XP_011510032.1:p.Thr22968Ile
|
|
XM_011511731.1:c.68762C>T
(TTN)
|
XP_011510033.1:p.Thr22921Ile
|
|
XM_017004819.1:c.94805C>T
(TTN)
|
XP_016860308.1:p.Thr31602Ile
|
|
XM_017004820.1:c.90203C>T
(TTN)
|
XP_016860309.1:p.Thr30068Ile
|
|
XM_017004821.1:c.90200C>T
(TTN)
|
XP_016860310.1:p.Thr30067Ile
|
|
XM_017004822.1:c.87242C>T
(TTN)
|
XP_016860311.1:p.Thr29081Ile
|
|
XM_017004823.1:c.68858C>T
(TTN)
|
XP_016860312.1:p.Thr22953Ile
|
|
XM_024453094.1:c.90353C>T
(TTN)
|
XP_024308862.1:p.Thr30118Ile
|
|
XM_024453095.1:c.90350C>T
(TTN)
|
XP_024308863.1:p.Thr30117Ile
|
|
XM_024453096.1:c.89783C>T
(TTN)
|
XP_024308864.1:p.Thr29928Ile
|
|
XM_024453097.1:c.87125C>T
(TTN)
|
XP_024308865.1:p.Thr29042Ile
|
|
XM_024453098.1:c.87044C>T
(TTN)
|
XP_024308866.1:p.Thr29015Ile
|
|
XM_024453099.1:c.68807C>T
(TTN)
|
XP_024308867.1:p.Thr22936Ile
|
|
XM_024453100.1:c.58661C>T
(TTN)
|
XP_024308868.1:p.Thr19554Ile
|
|