ENST00000342992.11:c.86999T>A
(TTN)
|
ENSP00000343764.6:p.Phe29000Tyr
|
|
ENST00000342175.11:c.68084T>A
(TTN)
|
ENSP00000340554.6:p.Phe22695Tyr
|
|
ENST00000359218.10:c.67883T>A
(TTN)
|
ENSP00000352154.5:p.Phe22628Tyr
|
|
ENST00000342175.10:c.68084T>A
(TTN)
|
ENSP00000340554.6:p.Phe22695Tyr
|
|
ENST00000342992.10:c.86999T>A
(TTN)
|
ENSP00000343764.6:p.Phe29000Tyr
|
|
ENST00000359218.9:c.67883T>A
(TTN)
|
ENSP00000352154.5:p.Phe22628Tyr
|
|
ENST00000460472.6:c.67508T>A
(TTN)
|
ENSP00000434586.1:p.Phe22503Tyr
|
|
ENST00000589042.5:c.94703T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe31568Tyr
|
|
ENST00000591111.5:c.89780T>A
(TTN)
|
ENSP00000465570.1:p.Phe29927Tyr
|
|
ENST00000615779.4:c.89780T>A
(TTN)
|
ENSP00000483597.1:p.Phe29927Tyr
|
|
NM_001256850.1:c.89780T>A
(TTN)
|
NP_001243779.1:p.Phe29927Tyr
|
|
NM_001267550.2:c.94703T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Phe31568Tyr
|
|
NM_003319.4:c.67508T>A
(TTN)
|
NP_003310.4:p.Phe22503Tyr
|
|
NM_133378.4:c.86999T>A
(TTN)
|
NP_596869.4:p.Phe29000Tyr
|
|
NM_133432.3:c.67883T>A
(TTN)
|
NP_597676.3:p.Phe22628Tyr
|
|
NM_133437.4:c.68084T>A
(TTN)
|
NP_597681.4:p.Phe22695Tyr
|
|
NR_038271.1:n.446+23089A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4364A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.93800T>A
(TTN)
|
XP_011510031.1:p.Phe31267Tyr
|
|
XM_011511730.1:c.67694T>A
(TTN)
|
XP_011510032.1:p.Phe22565Tyr
|
|
XM_011511731.1:c.67553T>A
(TTN)
|
XP_011510033.1:p.Phe22518Tyr
|
|
XM_017004819.1:c.93596T>A
(TTN)
|
XP_016860308.1:p.Phe31199Tyr
|
|
XM_017004820.1:c.88994T>A
(TTN)
|
XP_016860309.1:p.Phe29665Tyr
|
|
XM_017004821.1:c.88991T>A
(TTN)
|
XP_016860310.1:p.Phe29664Tyr
|
|
XM_017004822.1:c.86033T>A
(TTN)
|
XP_016860311.1:p.Phe28678Tyr
|
|
XM_017004823.1:c.67649T>A
(TTN)
|
XP_016860312.1:p.Phe22550Tyr
|
|
XM_024453094.1:c.89144T>A
(TTN)
|
XP_024308862.1:p.Phe29715Tyr
|
|
XM_024453095.1:c.89141T>A
(TTN)
|
XP_024308863.1:p.Phe29714Tyr
|
|
XM_024453096.1:c.88574T>A
(TTN)
|
XP_024308864.1:p.Phe29525Tyr
|
|
XM_024453097.1:c.85916T>A
(TTN)
|
XP_024308865.1:p.Phe28639Tyr
|
|
XM_024453098.1:c.85835T>A
(TTN)
|
XP_024308866.1:p.Phe28612Tyr
|
|
XM_024453099.1:c.67598T>A
(TTN)
|
XP_024308867.1:p.Phe22533Tyr
|
|
XM_024453100.1:c.57452T>A
(TTN)
|
XP_024308868.1:p.Phe19151Tyr
|
|