ENST00000342992.11:c.69591A>C
(TTN)
|
ENSP00000343764.6:p.Glu23197Asp
|
|
ENST00000342175.11:c.50676A>C
(TTN)
|
ENSP00000340554.6:p.Glu16892Asp
|
|
ENST00000359218.10:c.50475A>C
(TTN)
|
ENSP00000352154.5:p.Glu16825Asp
|
|
ENST00000342175.10:c.50676A>C
(TTN)
|
ENSP00000340554.6:p.Glu16892Asp
|
|
ENST00000342992.10:c.69591A>C
(TTN)
|
ENSP00000343764.6:p.Glu23197Asp
|
|
ENST00000359218.9:c.50475A>C
(TTN)
|
ENSP00000352154.5:p.Glu16825Asp
|
|
ENST00000460472.6:c.50100A>C
(TTN)
|
ENSP00000434586.1:p.Glu16700Asp
|
|
ENST00000589042.5:c.77295A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu25765Asp
|
|
ENST00000591111.5:c.72372A>C
(TTN)
|
ENSP00000465570.1:p.Glu24124Asp
|
|
ENST00000615779.4:c.72372A>C
(TTN)
|
ENSP00000483597.1:p.Glu24124Asp
|
|
NM_001256850.1:c.72372A>C
(TTN)
|
NP_001243779.1:p.Glu24124Asp
|
|
NM_001267550.2:c.77295A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu25765Asp
|
|
NM_003319.4:c.50100A>C
(TTN)
|
NP_003310.4:p.Glu16700Asp
|
|
NM_133378.4:c.69591A>C
(TTN)
|
NP_596869.4:p.Glu23197Asp
|
|
NM_133432.3:c.50475A>C
(TTN)
|
NP_597676.3:p.Glu16825Asp
|
|
NM_133437.4:c.50676A>C
(TTN)
|
NP_597681.4:p.Glu16892Asp
|
|
NR_038271.1:n.447-2463T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13735T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76392A>C
(TTN)
|
XP_011510031.1:p.Glu25464Asp
|
|
XM_011511730.1:c.50286A>C
(TTN)
|
XP_011510032.1:p.Glu16762Asp
|
|
XM_011511731.1:c.50145A>C
(TTN)
|
XP_011510033.1:p.Glu16715Asp
|
|
XM_017004819.1:c.76188A>C
(TTN)
|
XP_016860308.1:p.Glu25396Asp
|
|
XM_017004820.1:c.71586A>C
(TTN)
|
XP_016860309.1:p.Glu23862Asp
|
|
XM_017004821.1:c.71583A>C
(TTN)
|
XP_016860310.1:p.Glu23861Asp
|
|
XM_017004822.1:c.68625A>C
(TTN)
|
XP_016860311.1:p.Glu22875Asp
|
|
XM_017004823.1:c.50241A>C
(TTN)
|
XP_016860312.1:p.Glu16747Asp
|
|
XM_024453094.1:c.71736A>C
(TTN)
|
XP_024308862.1:p.Glu23912Asp
|
|
XM_024453095.1:c.71733A>C
(TTN)
|
XP_024308863.1:p.Glu23911Asp
|
|
XM_024453096.1:c.71166A>C
(TTN)
|
XP_024308864.1:p.Glu23722Asp
|
|
XM_024453097.1:c.68508A>C
(TTN)
|
XP_024308865.1:p.Glu22836Asp
|
|
XM_024453098.1:c.68427A>C
(TTN)
|
XP_024308866.1:p.Glu22809Asp
|
|
XM_024453099.1:c.50190A>C
(TTN)
|
XP_024308867.1:p.Glu16730Asp
|
|
XM_024453100.1:c.40044A>C
(TTN)
|
XP_024308868.1:p.Glu13348Asp
|
|