ENST00000342992.11:c.69436A>C
(TTN)
|
ENSP00000343764.6:p.Ser23146Arg
|
|
ENST00000342175.11:c.50521A>C
(TTN)
|
ENSP00000340554.6:p.Ser16841Arg
|
|
ENST00000359218.10:c.50320A>C
(TTN)
|
ENSP00000352154.5:p.Ser16774Arg
|
|
ENST00000342175.10:c.50521A>C
(TTN)
|
ENSP00000340554.6:p.Ser16841Arg
|
|
ENST00000342992.10:c.69436A>C
(TTN)
|
ENSP00000343764.6:p.Ser23146Arg
|
|
ENST00000359218.9:c.50320A>C
(TTN)
|
ENSP00000352154.5:p.Ser16774Arg
|
|
ENST00000460472.6:c.49945A>C
(TTN)
|
ENSP00000434586.1:p.Ser16649Arg
|
|
ENST00000589042.5:c.77140A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser25714Arg
|
|
ENST00000591111.5:c.72217A>C
(TTN)
|
ENSP00000465570.1:p.Ser24073Arg
|
|
ENST00000615779.4:c.72217A>C
(TTN)
|
ENSP00000483597.1:p.Ser24073Arg
|
|
NM_001256850.1:c.72217A>C
(TTN)
|
NP_001243779.1:p.Ser24073Arg
|
|
NM_001267550.2:c.77140A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser25714Arg
|
|
NM_003319.4:c.49945A>C
(TTN)
|
NP_003310.4:p.Ser16649Arg
|
|
NM_133378.4:c.69436A>C
(TTN)
|
NP_596869.4:p.Ser23146Arg
|
|
NM_133432.3:c.50320A>C
(TTN)
|
NP_597676.3:p.Ser16774Arg
|
|
NM_133437.4:c.50521A>C
(TTN)
|
NP_597681.4:p.Ser16841Arg
|
|
NR_038271.1:n.447-2308T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13580T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76237A>C
(TTN)
|
XP_011510031.1:p.Ser25413Arg
|
|
XM_011511730.1:c.50131A>C
(TTN)
|
XP_011510032.1:p.Ser16711Arg
|
|
XM_011511731.1:c.49990A>C
(TTN)
|
XP_011510033.1:p.Ser16664Arg
|
|
XM_017004819.1:c.76033A>C
(TTN)
|
XP_016860308.1:p.Ser25345Arg
|
|
XM_017004820.1:c.71431A>C
(TTN)
|
XP_016860309.1:p.Ser23811Arg
|
|
XM_017004821.1:c.71428A>C
(TTN)
|
XP_016860310.1:p.Ser23810Arg
|
|
XM_017004822.1:c.68470A>C
(TTN)
|
XP_016860311.1:p.Ser22824Arg
|
|
XM_017004823.1:c.50086A>C
(TTN)
|
XP_016860312.1:p.Ser16696Arg
|
|
XM_024453094.1:c.71581A>C
(TTN)
|
XP_024308862.1:p.Ser23861Arg
|
|
XM_024453095.1:c.71578A>C
(TTN)
|
XP_024308863.1:p.Ser23860Arg
|
|
XM_024453096.1:c.71011A>C
(TTN)
|
XP_024308864.1:p.Ser23671Arg
|
|
XM_024453097.1:c.68353A>C
(TTN)
|
XP_024308865.1:p.Ser22785Arg
|
|
XM_024453098.1:c.68272A>C
(TTN)
|
XP_024308866.1:p.Ser22758Arg
|
|
XM_024453099.1:c.50035A>C
(TTN)
|
XP_024308867.1:p.Ser16679Arg
|
|
XM_024453100.1:c.39889A>C
(TTN)
|
XP_024308868.1:p.Ser13297Arg
|
|