ENST00000342992.11:c.82701T>C
(TTN)
|
ENSP00000343764.6:p.Asp27567=
|
|
ENST00000342175.11:c.63786T>C
(TTN)
|
ENSP00000340554.6:p.Asp21262=
|
|
ENST00000359218.10:c.63585T>C
(TTN)
|
ENSP00000352154.5:p.Asp21195=
|
|
ENST00000342175.10:c.63786T>C
(TTN)
|
ENSP00000340554.6:p.Asp21262=
|
|
ENST00000342992.10:c.82701T>C
(TTN)
|
ENSP00000343764.6:p.Asp27567=
|
|
ENST00000359218.9:c.63585T>C
(TTN)
|
ENSP00000352154.5:p.Asp21195=
|
|
ENST00000460472.6:c.63210T>C
(TTN)
|
ENSP00000434586.1:p.Asp21070=
|
|
ENST00000589042.5:c.90405T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp30135=
|
|
ENST00000591111.5:c.85482T>C
(TTN)
|
ENSP00000465570.1:p.Asp28494=
|
|
ENST00000615779.4:c.85482T>C
(TTN)
|
ENSP00000483597.1:p.Asp28494=
|
|
NM_001256850.1:c.85482T>C
(TTN)
|
NP_001243779.1:p.Asp28494=
|
|
NM_001267550.2:c.90405T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp30135=
|
|
NM_003319.4:c.63210T>C
(TTN)
|
NP_003310.4:p.Asp21070=
|
|
NM_133378.4:c.82701T>C
(TTN)
|
NP_596869.4:p.Asp27567=
|
|
NM_133432.3:c.63585T>C
(TTN)
|
NP_597676.3:p.Asp21195=
|
|
NM_133437.4:c.63786T>C
(TTN)
|
NP_597681.4:p.Asp21262=
|
|
NR_038271.1:n.447-18805A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10134A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.89502T>C
(TTN)
|
XP_011510031.1:p.Asp29834=
|
|
XM_011511730.1:c.63396T>C
(TTN)
|
XP_011510032.1:p.Asp21132=
|
|
XM_011511731.1:c.63255T>C
(TTN)
|
XP_011510033.1:p.Asp21085=
|
|
XM_017004819.1:c.89298T>C
(TTN)
|
XP_016860308.1:p.Asp29766=
|
|
XM_017004820.1:c.84696T>C
(TTN)
|
XP_016860309.1:p.Asp28232=
|
|
XM_017004821.1:c.84693T>C
(TTN)
|
XP_016860310.1:p.Asp28231=
|
|
XM_017004822.1:c.81735T>C
(TTN)
|
XP_016860311.1:p.Asp27245=
|
|
XM_017004823.1:c.63351T>C
(TTN)
|
XP_016860312.1:p.Asp21117=
|
|
XM_024453094.1:c.84846T>C
(TTN)
|
XP_024308862.1:p.Asp28282=
|
|
XM_024453095.1:c.84843T>C
(TTN)
|
XP_024308863.1:p.Asp28281=
|
|
XM_024453096.1:c.84276T>C
(TTN)
|
XP_024308864.1:p.Asp28092=
|
|
XM_024453097.1:c.81618T>C
(TTN)
|
XP_024308865.1:p.Asp27206=
|
|
XM_024453098.1:c.81537T>C
(TTN)
|
XP_024308866.1:p.Asp27179=
|
|
XM_024453099.1:c.63300T>C
(TTN)
|
XP_024308867.1:p.Asp21100=
|
|
XM_024453100.1:c.53154T>C
(TTN)
|
XP_024308868.1:p.Asp17718=
|
|