ENST00000342992.11:c.88103A>T
(TTN)
|
ENSP00000343764.6:p.Asp29368Val
|
|
ENST00000342175.11:c.69188A>T
(TTN)
|
ENSP00000340554.6:p.Asp23063Val
|
|
ENST00000359218.10:c.68987A>T
(TTN)
|
ENSP00000352154.5:p.Asp22996Val
|
|
ENST00000342175.10:c.69188A>T
(TTN)
|
ENSP00000340554.6:p.Asp23063Val
|
|
ENST00000342992.10:c.88103A>T
(TTN)
|
ENSP00000343764.6:p.Asp29368Val
|
|
ENST00000359218.9:c.68987A>T
(TTN)
|
ENSP00000352154.5:p.Asp22996Val
|
|
ENST00000460472.6:c.68612A>T
(TTN)
|
ENSP00000434586.1:p.Asp22871Val
|
|
ENST00000589042.5:c.95807A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31936Val
|
|
ENST00000591111.5:c.90884A>T
(TTN)
|
ENSP00000465570.1:p.Asp30295Val
|
|
ENST00000615779.4:c.90884A>T
(TTN)
|
ENSP00000483597.1:p.Asp30295Val
|
|
NM_001256850.1:c.90884A>T
(TTN)
|
NP_001243779.1:p.Asp30295Val
|
|
NM_001267550.2:c.95807A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31936Val
|
|
NM_003319.4:c.68612A>T
(TTN)
|
NP_003310.4:p.Asp22871Val
|
|
NM_133378.4:c.88103A>T
(TTN)
|
NP_596869.4:p.Asp29368Val
|
|
NM_133432.3:c.68987A>T
(TTN)
|
NP_597676.3:p.Asp22996Val
|
|
NM_133437.4:c.69188A>T
(TTN)
|
NP_597681.4:p.Asp23063Val
|
|
NR_038271.1:n.446+20786T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2061T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.94904A>T
(TTN)
|
XP_011510031.1:p.Asp31635Val
|
|
XM_011511730.1:c.68798A>T
(TTN)
|
XP_011510032.1:p.Asp22933Val
|
|
XM_011511731.1:c.68657A>T
(TTN)
|
XP_011510033.1:p.Asp22886Val
|
|
XM_017004819.1:c.94700A>T
(TTN)
|
XP_016860308.1:p.Asp31567Val
|
|
XM_017004820.1:c.90098A>T
(TTN)
|
XP_016860309.1:p.Asp30033Val
|
|
XM_017004821.1:c.90095A>T
(TTN)
|
XP_016860310.1:p.Asp30032Val
|
|
XM_017004822.1:c.87137A>T
(TTN)
|
XP_016860311.1:p.Asp29046Val
|
|
XM_017004823.1:c.68753A>T
(TTN)
|
XP_016860312.1:p.Asp22918Val
|
|
XM_024453094.1:c.90248A>T
(TTN)
|
XP_024308862.1:p.Asp30083Val
|
|
XM_024453095.1:c.90245A>T
(TTN)
|
XP_024308863.1:p.Asp30082Val
|
|
XM_024453096.1:c.89678A>T
(TTN)
|
XP_024308864.1:p.Asp29893Val
|
|
XM_024453097.1:c.87020A>T
(TTN)
|
XP_024308865.1:p.Asp29007Val
|
|
XM_024453098.1:c.86939A>T
(TTN)
|
XP_024308866.1:p.Asp28980Val
|
|
XM_024453099.1:c.68702A>T
(TTN)
|
XP_024308867.1:p.Asp22901Val
|
|
XM_024453100.1:c.58556A>T
(TTN)
|
XP_024308868.1:p.Asp19519Val
|
|