ENST00000342992.11:c.98457A>T
(TTN)
|
ENSP00000343764.6:p.Ser32819=
|
|
ENST00000342175.11:c.79542A>T
(TTN)
|
ENSP00000340554.6:p.Ser26514=
|
|
ENST00000359218.10:c.79341A>T
(TTN)
|
ENSP00000352154.5:p.Ser26447=
|
|
ENST00000342175.10:c.79542A>T
(TTN)
|
ENSP00000340554.6:p.Ser26514=
|
|
ENST00000342992.10:c.98457A>T
(TTN)
|
ENSP00000343764.6:p.Ser32819=
|
|
ENST00000359218.9:c.79341A>T
(TTN)
|
ENSP00000352154.5:p.Ser26447=
|
|
ENST00000460472.6:c.78966A>T
(TTN)
|
ENSP00000434586.1:p.Ser26322=
|
|
ENST00000589042.5:c.106161A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35387=
|
|
ENST00000591111.5:c.101238A>T
(TTN)
|
ENSP00000465570.1:p.Ser33746=
|
|
ENST00000615779.4:c.101238A>T
(TTN)
|
ENSP00000483597.1:p.Ser33746=
|
|
NM_001256850.1:c.101238A>T
(TTN)
|
NP_001243779.1:p.Ser33746=
|
|
NM_001267550.2:c.106161A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35387=
|
|
NM_003319.4:c.78966A>T
(TTN)
|
NP_003310.4:p.Ser26322=
|
|
NM_133378.4:c.98457A>T
(TTN)
|
NP_596869.4:p.Ser32819=
|
|
NM_133432.3:c.79341A>T
(TTN)
|
NP_597676.3:p.Ser26447=
|
|
NM_133437.4:c.79542A>T
(TTN)
|
NP_597681.4:p.Ser26514=
|
|
NR_038271.1:n.446+6818T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5278T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105258A>T
(TTN)
|
XP_011510031.1:p.Ser35086=
|
|
XM_011511730.1:c.79152A>T
(TTN)
|
XP_011510032.1:p.Ser26384=
|
|
XM_011511731.1:c.79011A>T
(TTN)
|
XP_011510033.1:p.Ser26337=
|
|
XM_017004819.1:c.105054A>T
(TTN)
|
XP_016860308.1:p.Ser35018=
|
|
XM_017004820.1:c.100452A>T
(TTN)
|
XP_016860309.1:p.Ser33484=
|
|
XM_017004821.1:c.100449A>T
(TTN)
|
XP_016860310.1:p.Ser33483=
|
|
XM_017004822.1:c.97491A>T
(TTN)
|
XP_016860311.1:p.Ser32497=
|
|
XM_017004823.1:c.79107A>T
(TTN)
|
XP_016860312.1:p.Ser26369=
|
|
XM_024453094.1:c.100602A>T
(TTN)
|
XP_024308862.1:p.Ser33534=
|
|
XM_024453095.1:c.100599A>T
(TTN)
|
XP_024308863.1:p.Ser33533=
|
|
XM_024453096.1:c.100032A>T
(TTN)
|
XP_024308864.1:p.Ser33344=
|
|
XM_024453097.1:c.97374A>T
(TTN)
|
XP_024308865.1:p.Ser32458=
|
|
XM_024453098.1:c.97293A>T
(TTN)
|
XP_024308866.1:p.Ser32431=
|
|
XM_024453099.1:c.79056A>T
(TTN)
|
XP_024308867.1:p.Ser26352=
|
|
XM_024453100.1:c.68910A>T
(TTN)
|
XP_024308868.1:p.Ser22970=
|
|