ENST00000342992.11:c.76118A>T
(TTN)
|
ENSP00000343764.6:p.Glu25373Val
|
|
ENST00000342175.11:c.57203A>T
(TTN)
|
ENSP00000340554.6:p.Glu19068Val
|
|
ENST00000359218.10:c.57002A>T
(TTN)
|
ENSP00000352154.5:p.Glu19001Val
|
|
ENST00000342175.10:c.57203A>T
(TTN)
|
ENSP00000340554.6:p.Glu19068Val
|
|
ENST00000342992.10:c.76118A>T
(TTN)
|
ENSP00000343764.6:p.Glu25373Val
|
|
ENST00000359218.9:c.57002A>T
(TTN)
|
ENSP00000352154.5:p.Glu19001Val
|
|
ENST00000460472.6:c.56627A>T
(TTN)
|
ENSP00000434586.1:p.Glu18876Val
|
|
ENST00000589042.5:c.83822A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu27941Val
|
|
ENST00000591111.5:c.78899A>T
(TTN)
|
ENSP00000465570.1:p.Glu26300Val
|
|
ENST00000615779.4:c.78899A>T
(TTN)
|
ENSP00000483597.1:p.Glu26300Val
|
|
NM_001256850.1:c.78899A>T
(TTN)
|
NP_001243779.1:p.Glu26300Val
|
|
NM_001267550.2:c.83822A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu27941Val
|
|
NM_003319.4:c.56627A>T
(TTN)
|
NP_003310.4:p.Glu18876Val
|
|
NM_133378.4:c.76118A>T
(TTN)
|
NP_596869.4:p.Glu25373Val
|
|
NM_133432.3:c.57002A>T
(TTN)
|
NP_597676.3:p.Glu19001Val
|
|
NM_133437.4:c.57203A>T
(TTN)
|
NP_597681.4:p.Glu19068Val
|
|
NR_038271.1:n.447-8990T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+19949T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.82919A>T
(TTN)
|
XP_011510031.1:p.Glu27640Val
|
|
XM_011511730.1:c.56813A>T
(TTN)
|
XP_011510032.1:p.Glu18938Val
|
|
XM_011511731.1:c.56672A>T
(TTN)
|
XP_011510033.1:p.Glu18891Val
|
|
XM_017004819.1:c.82715A>T
(TTN)
|
XP_016860308.1:p.Glu27572Val
|
|
XM_017004820.1:c.78113A>T
(TTN)
|
XP_016860309.1:p.Glu26038Val
|
|
XM_017004821.1:c.78110A>T
(TTN)
|
XP_016860310.1:p.Glu26037Val
|
|
XM_017004822.1:c.75152A>T
(TTN)
|
XP_016860311.1:p.Glu25051Val
|
|
XM_017004823.1:c.56768A>T
(TTN)
|
XP_016860312.1:p.Glu18923Val
|
|
XM_024453094.1:c.78263A>T
(TTN)
|
XP_024308862.1:p.Glu26088Val
|
|
XM_024453095.1:c.78260A>T
(TTN)
|
XP_024308863.1:p.Glu26087Val
|
|
XM_024453096.1:c.77693A>T
(TTN)
|
XP_024308864.1:p.Glu25898Val
|
|
XM_024453097.1:c.75035A>T
(TTN)
|
XP_024308865.1:p.Glu25012Val
|
|
XM_024453098.1:c.74954A>T
(TTN)
|
XP_024308866.1:p.Glu24985Val
|
|
XM_024453099.1:c.56717A>T
(TTN)
|
XP_024308867.1:p.Glu18906Val
|
|
XM_024453100.1:c.46571A>T
(TTN)
|
XP_024308868.1:p.Glu15524Val
|
|