ENST00000342992.11:c.88957C>A
(TTN)
|
ENSP00000343764.6:p.Leu29653Ile
|
|
ENST00000342175.11:c.70042C>A
(TTN)
|
ENSP00000340554.6:p.Leu23348Ile
|
|
ENST00000359218.10:c.69841C>A
(TTN)
|
ENSP00000352154.5:p.Leu23281Ile
|
|
ENST00000342175.10:c.70042C>A
(TTN)
|
ENSP00000340554.6:p.Leu23348Ile
|
|
ENST00000342992.10:c.88957C>A
(TTN)
|
ENSP00000343764.6:p.Leu29653Ile
|
|
ENST00000359218.9:c.69841C>A
(TTN)
|
ENSP00000352154.5:p.Leu23281Ile
|
|
ENST00000460472.6:c.69466C>A
(TTN)
|
ENSP00000434586.1:p.Leu23156Ile
|
|
ENST00000589042.5:c.96661C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32221Ile
|
|
ENST00000591111.5:c.91738C>A
(TTN)
|
ENSP00000465570.1:p.Leu30580Ile
|
|
ENST00000615779.4:c.91738C>A
(TTN)
|
ENSP00000483597.1:p.Leu30580Ile
|
|
NM_001256850.1:c.91738C>A
(TTN)
|
NP_001243779.1:p.Leu30580Ile
|
|
NM_001267550.2:c.96661C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32221Ile
|
|
NM_003319.4:c.69466C>A
(TTN)
|
NP_003310.4:p.Leu23156Ile
|
|
NM_133378.4:c.88957C>A
(TTN)
|
NP_596869.4:p.Leu29653Ile
|
|
NM_133432.3:c.69841C>A
(TTN)
|
NP_597676.3:p.Leu23281Ile
|
|
NM_133437.4:c.70042C>A
(TTN)
|
NP_597681.4:p.Leu23348Ile
|
|
NR_038271.1:n.446+19676G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+951G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.95758C>A
(TTN)
|
XP_011510031.1:p.Leu31920Ile
|
|
XM_011511730.1:c.69652C>A
(TTN)
|
XP_011510032.1:p.Leu23218Ile
|
|
XM_011511731.1:c.69511C>A
(TTN)
|
XP_011510033.1:p.Leu23171Ile
|
|
XM_017004819.1:c.95554C>A
(TTN)
|
XP_016860308.1:p.Leu31852Ile
|
|
XM_017004820.1:c.90952C>A
(TTN)
|
XP_016860309.1:p.Leu30318Ile
|
|
XM_017004821.1:c.90949C>A
(TTN)
|
XP_016860310.1:p.Leu30317Ile
|
|
XM_017004822.1:c.87991C>A
(TTN)
|
XP_016860311.1:p.Leu29331Ile
|
|
XM_017004823.1:c.69607C>A
(TTN)
|
XP_016860312.1:p.Leu23203Ile
|
|
XM_024453094.1:c.91102C>A
(TTN)
|
XP_024308862.1:p.Leu30368Ile
|
|
XM_024453095.1:c.91099C>A
(TTN)
|
XP_024308863.1:p.Leu30367Ile
|
|
XM_024453096.1:c.90532C>A
(TTN)
|
XP_024308864.1:p.Leu30178Ile
|
|
XM_024453097.1:c.87874C>A
(TTN)
|
XP_024308865.1:p.Leu29292Ile
|
|
XM_024453098.1:c.87793C>A
(TTN)
|
XP_024308866.1:p.Leu29265Ile
|
|
XM_024453099.1:c.69556C>A
(TTN)
|
XP_024308867.1:p.Leu23186Ile
|
|
XM_024453100.1:c.59410C>A
(TTN)
|
XP_024308868.1:p.Leu19804Ile
|
|