ENST00000342992.11:c.88219C>A
(TTN)
|
ENSP00000343764.6:p.Leu29407Ile
|
|
ENST00000342175.11:c.69304C>A
(TTN)
|
ENSP00000340554.6:p.Leu23102Ile
|
|
ENST00000359218.10:c.69103C>A
(TTN)
|
ENSP00000352154.5:p.Leu23035Ile
|
|
ENST00000342175.10:c.69304C>A
(TTN)
|
ENSP00000340554.6:p.Leu23102Ile
|
|
ENST00000342992.10:c.88219C>A
(TTN)
|
ENSP00000343764.6:p.Leu29407Ile
|
|
ENST00000359218.9:c.69103C>A
(TTN)
|
ENSP00000352154.5:p.Leu23035Ile
|
|
ENST00000460472.6:c.68728C>A
(TTN)
|
ENSP00000434586.1:p.Leu22910Ile
|
|
ENST00000589042.5:c.95923C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu31975Ile
|
|
ENST00000591111.5:c.91000C>A
(TTN)
|
ENSP00000465570.1:p.Leu30334Ile
|
|
ENST00000615779.4:c.91000C>A
(TTN)
|
ENSP00000483597.1:p.Leu30334Ile
|
|
NM_001256850.1:c.91000C>A
(TTN)
|
NP_001243779.1:p.Leu30334Ile
|
|
NM_001267550.2:c.95923C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu31975Ile
|
|
NM_003319.4:c.68728C>A
(TTN)
|
NP_003310.4:p.Leu22910Ile
|
|
NM_133378.4:c.88219C>A
(TTN)
|
NP_596869.4:p.Leu29407Ile
|
|
NM_133432.3:c.69103C>A
(TTN)
|
NP_597676.3:p.Leu23035Ile
|
|
NM_133437.4:c.69304C>A
(TTN)
|
NP_597681.4:p.Leu23102Ile
|
|
NR_038271.1:n.446+20670G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1945G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.95020C>A
(TTN)
|
XP_011510031.1:p.Leu31674Ile
|
|
XM_011511730.1:c.68914C>A
(TTN)
|
XP_011510032.1:p.Leu22972Ile
|
|
XM_011511731.1:c.68773C>A
(TTN)
|
XP_011510033.1:p.Leu22925Ile
|
|
XM_017004819.1:c.94816C>A
(TTN)
|
XP_016860308.1:p.Leu31606Ile
|
|
XM_017004820.1:c.90214C>A
(TTN)
|
XP_016860309.1:p.Leu30072Ile
|
|
XM_017004821.1:c.90211C>A
(TTN)
|
XP_016860310.1:p.Leu30071Ile
|
|
XM_017004822.1:c.87253C>A
(TTN)
|
XP_016860311.1:p.Leu29085Ile
|
|
XM_017004823.1:c.68869C>A
(TTN)
|
XP_016860312.1:p.Leu22957Ile
|
|
XM_024453094.1:c.90364C>A
(TTN)
|
XP_024308862.1:p.Leu30122Ile
|
|
XM_024453095.1:c.90361C>A
(TTN)
|
XP_024308863.1:p.Leu30121Ile
|
|
XM_024453096.1:c.89794C>A
(TTN)
|
XP_024308864.1:p.Leu29932Ile
|
|
XM_024453097.1:c.87136C>A
(TTN)
|
XP_024308865.1:p.Leu29046Ile
|
|
XM_024453098.1:c.87055C>A
(TTN)
|
XP_024308866.1:p.Leu29019Ile
|
|
XM_024453099.1:c.68818C>A
(TTN)
|
XP_024308867.1:p.Leu22940Ile
|
|
XM_024453100.1:c.58672C>A
(TTN)
|
XP_024308868.1:p.Leu19558Ile
|
|