ENST00000342992.11:c.47357A>C
(TTN)
|
ENSP00000343764.6:p.Glu15786Ala
|
|
ENST00000342175.11:c.28442A>C
(TTN)
|
ENSP00000340554.6:p.Glu9481Ala
|
|
ENST00000359218.10:c.28241A>C
(TTN)
|
ENSP00000352154.5:p.Glu9414Ala
|
|
ENST00000342175.10:c.28442A>C
(TTN)
|
ENSP00000340554.6:p.Glu9481Ala
|
|
ENST00000342992.10:c.47357A>C
(TTN)
|
ENSP00000343764.6:p.Glu15786Ala
|
|
ENST00000359218.9:c.28241A>C
(TTN)
|
ENSP00000352154.5:p.Glu9414Ala
|
|
ENST00000460472.6:c.27866A>C
(TTN)
|
ENSP00000434586.1:p.Glu9289Ala
|
|
ENST00000589042.5:c.55061A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu18354Ala
|
|
ENST00000591111.5:c.50138A>C
(TTN)
|
ENSP00000465570.1:p.Glu16713Ala
|
|
ENST00000615779.4:c.50138A>C
(TTN)
|
ENSP00000483597.1:p.Glu16713Ala
|
|
NM_001256850.1:c.50138A>C
(TTN)
|
NP_001243779.1:p.Glu16713Ala
|
|
NM_001267550.2:c.55061A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu18354Ala
|
|
NM_003319.4:c.27866A>C
(TTN)
|
NP_003310.4:p.Glu9289Ala
|
|
NM_133378.4:c.47357A>C
(TTN)
|
NP_596869.4:p.Glu15786Ala
|
|
NM_133432.3:c.28241A>C
(TTN)
|
NP_597676.3:p.Glu9414Ala
|
|
NM_133437.4:c.28442A>C
(TTN)
|
NP_597681.4:p.Glu9481Ala
|
|
NR_038271.1:n.682+4660T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1674T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.54158A>C
(TTN)
|
XP_011510031.1:p.Glu18053Ala
|
|
XM_011511730.1:c.28052A>C
(TTN)
|
XP_011510032.1:p.Glu9351Ala
|
|
XM_011511731.1:c.27911A>C
(TTN)
|
XP_011510033.1:p.Glu9304Ala
|
|
XM_017004819.1:c.53954A>C
(TTN)
|
XP_016860308.1:p.Glu17985Ala
|
|
XM_017004820.1:c.49352A>C
(TTN)
|
XP_016860309.1:p.Glu16451Ala
|
|
XM_017004821.1:c.49349A>C
(TTN)
|
XP_016860310.1:p.Glu16450Ala
|
|
XM_017004822.1:c.46391A>C
(TTN)
|
XP_016860311.1:p.Glu15464Ala
|
|
XM_017004823.1:c.28007A>C
(TTN)
|
XP_016860312.1:p.Glu9336Ala
|
|
XM_024453094.1:c.49502A>C
(TTN)
|
XP_024308862.1:p.Glu16501Ala
|
|
XM_024453095.1:c.49499A>C
(TTN)
|
XP_024308863.1:p.Glu16500Ala
|
|
XM_024453096.1:c.48932A>C
(TTN)
|
XP_024308864.1:p.Glu16311Ala
|
|
XM_024453097.1:c.46274A>C
(TTN)
|
XP_024308865.1:p.Glu15425Ala
|
|
XM_024453098.1:c.46193A>C
(TTN)
|
XP_024308866.1:p.Glu15398Ala
|
|
XM_024453099.1:c.27956A>C
(TTN)
|
XP_024308867.1:p.Glu9319Ala
|
|
XM_024453100.1:c.17810A>C
(TTN)
|
XP_024308868.1:p.Glu5937Ala
|
|