ENST00000342992.11:c.85264G>T
(TTN)
|
ENSP00000343764.6:p.Asp28422Tyr
|
|
ENST00000342175.11:c.66349G>T
(TTN)
|
ENSP00000340554.6:p.Asp22117Tyr
|
|
ENST00000359218.10:c.66148G>T
(TTN)
|
ENSP00000352154.5:p.Asp22050Tyr
|
|
ENST00000342175.10:c.66349G>T
(TTN)
|
ENSP00000340554.6:p.Asp22117Tyr
|
|
ENST00000342992.10:c.85264G>T
(TTN)
|
ENSP00000343764.6:p.Asp28422Tyr
|
|
ENST00000359218.9:c.66148G>T
(TTN)
|
ENSP00000352154.5:p.Asp22050Tyr
|
|
ENST00000460472.6:c.65773G>T
(TTN)
|
ENSP00000434586.1:p.Asp21925Tyr
|
|
ENST00000589042.5:c.92968G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp30990Tyr
|
|
ENST00000591111.5:c.88045G>T
(TTN)
|
ENSP00000465570.1:p.Asp29349Tyr
|
|
ENST00000615779.4:c.88045G>T
(TTN)
|
ENSP00000483597.1:p.Asp29349Tyr
|
|
NM_001256850.1:c.88045G>T
(TTN)
|
NP_001243779.1:p.Asp29349Tyr
|
|
NM_001267550.2:c.92968G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp30990Tyr
|
|
NM_003319.4:c.65773G>T
(TTN)
|
NP_003310.4:p.Asp21925Tyr
|
|
NM_133378.4:c.85264G>T
(TTN)
|
NP_596869.4:p.Asp28422Tyr
|
|
NM_133432.3:c.66148G>T
(TTN)
|
NP_597676.3:p.Asp22050Tyr
|
|
NM_133437.4:c.66349G>T
(TTN)
|
NP_597681.4:p.Asp22117Tyr
|
|
NR_038271.1:n.447-22642C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6297C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.92065G>T
(TTN)
|
XP_011510031.1:p.Asp30689Tyr
|
|
XM_011511730.1:c.65959G>T
(TTN)
|
XP_011510032.1:p.Asp21987Tyr
|
|
XM_011511731.1:c.65818G>T
(TTN)
|
XP_011510033.1:p.Asp21940Tyr
|
|
XM_017004819.1:c.91861G>T
(TTN)
|
XP_016860308.1:p.Asp30621Tyr
|
|
XM_017004820.1:c.87259G>T
(TTN)
|
XP_016860309.1:p.Asp29087Tyr
|
|
XM_017004821.1:c.87256G>T
(TTN)
|
XP_016860310.1:p.Asp29086Tyr
|
|
XM_017004822.1:c.84298G>T
(TTN)
|
XP_016860311.1:p.Asp28100Tyr
|
|
XM_017004823.1:c.65914G>T
(TTN)
|
XP_016860312.1:p.Asp21972Tyr
|
|
XM_024453094.1:c.87409G>T
(TTN)
|
XP_024308862.1:p.Asp29137Tyr
|
|
XM_024453095.1:c.87406G>T
(TTN)
|
XP_024308863.1:p.Asp29136Tyr
|
|
XM_024453096.1:c.86839G>T
(TTN)
|
XP_024308864.1:p.Asp28947Tyr
|
|
XM_024453097.1:c.84181G>T
(TTN)
|
XP_024308865.1:p.Asp28061Tyr
|
|
XM_024453098.1:c.84100G>T
(TTN)
|
XP_024308866.1:p.Asp28034Tyr
|
|
XM_024453099.1:c.65863G>T
(TTN)
|
XP_024308867.1:p.Asp21955Tyr
|
|
XM_024453100.1:c.55717G>T
(TTN)
|
XP_024308868.1:p.Asp18573Tyr
|
|