ENST00000342992.11:c.88603T>C
(TTN)
|
ENSP00000343764.6:p.Tyr29535His
|
|
ENST00000342175.11:c.69688T>C
(TTN)
|
ENSP00000340554.6:p.Tyr23230His
|
|
ENST00000359218.10:c.69487T>C
(TTN)
|
ENSP00000352154.5:p.Tyr23163His
|
|
ENST00000342175.10:c.69688T>C
(TTN)
|
ENSP00000340554.6:p.Tyr23230His
|
|
ENST00000342992.10:c.88603T>C
(TTN)
|
ENSP00000343764.6:p.Tyr29535His
|
|
ENST00000359218.9:c.69487T>C
(TTN)
|
ENSP00000352154.5:p.Tyr23163His
|
|
ENST00000460472.6:c.69112T>C
(TTN)
|
ENSP00000434586.1:p.Tyr23038His
|
|
ENST00000589042.5:c.96307T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr32103His
|
|
ENST00000591111.5:c.91384T>C
(TTN)
|
ENSP00000465570.1:p.Tyr30462His
|
|
ENST00000615779.4:c.91384T>C
(TTN)
|
ENSP00000483597.1:p.Tyr30462His
|
|
NM_001256850.1:c.91384T>C
(TTN)
|
NP_001243779.1:p.Tyr30462His
|
|
NM_001267550.2:c.96307T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr32103His
|
|
NM_003319.4:c.69112T>C
(TTN)
|
NP_003310.4:p.Tyr23038His
|
|
NM_133378.4:c.88603T>C
(TTN)
|
NP_596869.4:p.Tyr29535His
|
|
NM_133432.3:c.69487T>C
(TTN)
|
NP_597676.3:p.Tyr23163His
|
|
NM_133437.4:c.69688T>C
(TTN)
|
NP_597681.4:p.Tyr23230His
|
|
NR_038271.1:n.446+20201A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1476A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95404T>C
(TTN)
|
XP_011510031.1:p.Tyr31802His
|
|
XM_011511730.1:c.69298T>C
(TTN)
|
XP_011510032.1:p.Tyr23100His
|
|
XM_011511731.1:c.69157T>C
(TTN)
|
XP_011510033.1:p.Tyr23053His
|
|
XM_017004819.1:c.95200T>C
(TTN)
|
XP_016860308.1:p.Tyr31734His
|
|
XM_017004820.1:c.90598T>C
(TTN)
|
XP_016860309.1:p.Tyr30200His
|
|
XM_017004821.1:c.90595T>C
(TTN)
|
XP_016860310.1:p.Tyr30199His
|
|
XM_017004822.1:c.87637T>C
(TTN)
|
XP_016860311.1:p.Tyr29213His
|
|
XM_017004823.1:c.69253T>C
(TTN)
|
XP_016860312.1:p.Tyr23085His
|
|
XM_024453094.1:c.90748T>C
(TTN)
|
XP_024308862.1:p.Tyr30250His
|
|
XM_024453095.1:c.90745T>C
(TTN)
|
XP_024308863.1:p.Tyr30249His
|
|
XM_024453096.1:c.90178T>C
(TTN)
|
XP_024308864.1:p.Tyr30060His
|
|
XM_024453097.1:c.87520T>C
(TTN)
|
XP_024308865.1:p.Tyr29174His
|
|
XM_024453098.1:c.87439T>C
(TTN)
|
XP_024308866.1:p.Tyr29147His
|
|
XM_024453099.1:c.69202T>C
(TTN)
|
XP_024308867.1:p.Tyr23068His
|
|
XM_024453100.1:c.59056T>C
(TTN)
|
XP_024308868.1:p.Tyr19686His
|
|