ENST00000342992.11:c.69320T>A
(TTN)
|
ENSP00000343764.6:p.Val23107Asp
|
|
ENST00000342175.11:c.50405T>A
(TTN)
|
ENSP00000340554.6:p.Val16802Asp
|
|
ENST00000359218.10:c.50204T>A
(TTN)
|
ENSP00000352154.5:p.Val16735Asp
|
|
ENST00000342175.10:c.50405T>A
(TTN)
|
ENSP00000340554.6:p.Val16802Asp
|
|
ENST00000342992.10:c.69320T>A
(TTN)
|
ENSP00000343764.6:p.Val23107Asp
|
|
ENST00000359218.9:c.50204T>A
(TTN)
|
ENSP00000352154.5:p.Val16735Asp
|
|
ENST00000460472.6:c.49829T>A
(TTN)
|
ENSP00000434586.1:p.Val16610Asp
|
|
ENST00000589042.5:c.77024T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val25675Asp
|
|
ENST00000591111.5:c.72101T>A
(TTN)
|
ENSP00000465570.1:p.Val24034Asp
|
|
ENST00000615779.4:c.72101T>A
(TTN)
|
ENSP00000483597.1:p.Val24034Asp
|
|
NM_001256850.1:c.72101T>A
(TTN)
|
NP_001243779.1:p.Val24034Asp
|
|
NM_001267550.2:c.77024T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Val25675Asp
|
|
NM_003319.4:c.49829T>A
(TTN)
|
NP_003310.4:p.Val16610Asp
|
|
NM_133378.4:c.69320T>A
(TTN)
|
NP_596869.4:p.Val23107Asp
|
|
NM_133432.3:c.50204T>A
(TTN)
|
NP_597676.3:p.Val16735Asp
|
|
NM_133437.4:c.50405T>A
(TTN)
|
NP_597681.4:p.Val16802Asp
|
|
NR_038271.1:n.447-2192A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13464A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.76121T>A
(TTN)
|
XP_011510031.1:p.Val25374Asp
|
|
XM_011511730.1:c.50015T>A
(TTN)
|
XP_011510032.1:p.Val16672Asp
|
|
XM_011511731.1:c.49874T>A
(TTN)
|
XP_011510033.1:p.Val16625Asp
|
|
XM_017004819.1:c.75917T>A
(TTN)
|
XP_016860308.1:p.Val25306Asp
|
|
XM_017004820.1:c.71315T>A
(TTN)
|
XP_016860309.1:p.Val23772Asp
|
|
XM_017004821.1:c.71312T>A
(TTN)
|
XP_016860310.1:p.Val23771Asp
|
|
XM_017004822.1:c.68354T>A
(TTN)
|
XP_016860311.1:p.Val22785Asp
|
|
XM_017004823.1:c.49970T>A
(TTN)
|
XP_016860312.1:p.Val16657Asp
|
|
XM_024453094.1:c.71465T>A
(TTN)
|
XP_024308862.1:p.Val23822Asp
|
|
XM_024453095.1:c.71462T>A
(TTN)
|
XP_024308863.1:p.Val23821Asp
|
|
XM_024453096.1:c.70895T>A
(TTN)
|
XP_024308864.1:p.Val23632Asp
|
|
XM_024453097.1:c.68237T>A
(TTN)
|
XP_024308865.1:p.Val22746Asp
|
|
XM_024453098.1:c.68156T>A
(TTN)
|
XP_024308866.1:p.Val22719Asp
|
|
XM_024453099.1:c.49919T>A
(TTN)
|
XP_024308867.1:p.Val16640Asp
|
|
XM_024453100.1:c.39773T>A
(TTN)
|
XP_024308868.1:p.Val13258Asp
|
|