ENST00000342992.11:c.85266T>G
(TTN)
|
ENSP00000343764.6:p.Asp28422Glu
|
|
ENST00000342175.11:c.66351T>G
(TTN)
|
ENSP00000340554.6:p.Asp22117Glu
|
|
ENST00000359218.10:c.66150T>G
(TTN)
|
ENSP00000352154.5:p.Asp22050Glu
|
|
ENST00000342175.10:c.66351T>G
(TTN)
|
ENSP00000340554.6:p.Asp22117Glu
|
|
ENST00000342992.10:c.85266T>G
(TTN)
|
ENSP00000343764.6:p.Asp28422Glu
|
|
ENST00000359218.9:c.66150T>G
(TTN)
|
ENSP00000352154.5:p.Asp22050Glu
|
|
ENST00000460472.6:c.65775T>G
(TTN)
|
ENSP00000434586.1:p.Asp21925Glu
|
|
ENST00000589042.5:c.92970T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp30990Glu
|
|
ENST00000591111.5:c.88047T>G
(TTN)
|
ENSP00000465570.1:p.Asp29349Glu
|
|
ENST00000615779.4:c.88047T>G
(TTN)
|
ENSP00000483597.1:p.Asp29349Glu
|
|
NM_001256850.1:c.88047T>G
(TTN)
|
NP_001243779.1:p.Asp29349Glu
|
|
NM_001267550.2:c.92970T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp30990Glu
|
|
NM_003319.4:c.65775T>G
(TTN)
|
NP_003310.4:p.Asp21925Glu
|
|
NM_133378.4:c.85266T>G
(TTN)
|
NP_596869.4:p.Asp28422Glu
|
|
NM_133432.3:c.66150T>G
(TTN)
|
NP_597676.3:p.Asp22050Glu
|
|
NM_133437.4:c.66351T>G
(TTN)
|
NP_597681.4:p.Asp22117Glu
|
|
NR_038271.1:n.447-22644A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6295A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.92067T>G
(TTN)
|
XP_011510031.1:p.Asp30689Glu
|
|
XM_011511730.1:c.65961T>G
(TTN)
|
XP_011510032.1:p.Asp21987Glu
|
|
XM_011511731.1:c.65820T>G
(TTN)
|
XP_011510033.1:p.Asp21940Glu
|
|
XM_017004819.1:c.91863T>G
(TTN)
|
XP_016860308.1:p.Asp30621Glu
|
|
XM_017004820.1:c.87261T>G
(TTN)
|
XP_016860309.1:p.Asp29087Glu
|
|
XM_017004821.1:c.87258T>G
(TTN)
|
XP_016860310.1:p.Asp29086Glu
|
|
XM_017004822.1:c.84300T>G
(TTN)
|
XP_016860311.1:p.Asp28100Glu
|
|
XM_017004823.1:c.65916T>G
(TTN)
|
XP_016860312.1:p.Asp21972Glu
|
|
XM_024453094.1:c.87411T>G
(TTN)
|
XP_024308862.1:p.Asp29137Glu
|
|
XM_024453095.1:c.87408T>G
(TTN)
|
XP_024308863.1:p.Asp29136Glu
|
|
XM_024453096.1:c.86841T>G
(TTN)
|
XP_024308864.1:p.Asp28947Glu
|
|
XM_024453097.1:c.84183T>G
(TTN)
|
XP_024308865.1:p.Asp28061Glu
|
|
XM_024453098.1:c.84102T>G
(TTN)
|
XP_024308866.1:p.Asp28034Glu
|
|
XM_024453099.1:c.65865T>G
(TTN)
|
XP_024308867.1:p.Asp21955Glu
|
|
XM_024453100.1:c.55719T>G
(TTN)
|
XP_024308868.1:p.Asp18573Glu
|
|