ENST00000342992.11:c.82620G>C
(TTN)
|
ENSP00000343764.6:p.Glu27540Asp
|
|
ENST00000342175.11:c.63705G>C
(TTN)
|
ENSP00000340554.6:p.Glu21235Asp
|
|
ENST00000359218.10:c.63504G>C
(TTN)
|
ENSP00000352154.5:p.Glu21168Asp
|
|
ENST00000342175.10:c.63705G>C
(TTN)
|
ENSP00000340554.6:p.Glu21235Asp
|
|
ENST00000342992.10:c.82620G>C
(TTN)
|
ENSP00000343764.6:p.Glu27540Asp
|
|
ENST00000359218.9:c.63504G>C
(TTN)
|
ENSP00000352154.5:p.Glu21168Asp
|
|
ENST00000460472.6:c.63129G>C
(TTN)
|
ENSP00000434586.1:p.Glu21043Asp
|
|
ENST00000589042.5:c.90324G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu30108Asp
|
|
ENST00000591111.5:c.85401G>C
(TTN)
|
ENSP00000465570.1:p.Glu28467Asp
|
|
ENST00000615779.4:c.85401G>C
(TTN)
|
ENSP00000483597.1:p.Glu28467Asp
|
|
NM_001256850.1:c.85401G>C
(TTN)
|
NP_001243779.1:p.Glu28467Asp
|
|
NM_001267550.2:c.90324G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu30108Asp
|
|
NM_003319.4:c.63129G>C
(TTN)
|
NP_003310.4:p.Glu21043Asp
|
|
NM_133378.4:c.82620G>C
(TTN)
|
NP_596869.4:p.Glu27540Asp
|
|
NM_133432.3:c.63504G>C
(TTN)
|
NP_597676.3:p.Glu21168Asp
|
|
NM_133437.4:c.63705G>C
(TTN)
|
NP_597681.4:p.Glu21235Asp
|
|
NR_038271.1:n.447-18724C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10215C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.89421G>C
(TTN)
|
XP_011510031.1:p.Glu29807Asp
|
|
XM_011511730.1:c.63315G>C
(TTN)
|
XP_011510032.1:p.Glu21105Asp
|
|
XM_011511731.1:c.63174G>C
(TTN)
|
XP_011510033.1:p.Glu21058Asp
|
|
XM_017004819.1:c.89217G>C
(TTN)
|
XP_016860308.1:p.Glu29739Asp
|
|
XM_017004820.1:c.84615G>C
(TTN)
|
XP_016860309.1:p.Glu28205Asp
|
|
XM_017004821.1:c.84612G>C
(TTN)
|
XP_016860310.1:p.Glu28204Asp
|
|
XM_017004822.1:c.81654G>C
(TTN)
|
XP_016860311.1:p.Glu27218Asp
|
|
XM_017004823.1:c.63270G>C
(TTN)
|
XP_016860312.1:p.Glu21090Asp
|
|
XM_024453094.1:c.84765G>C
(TTN)
|
XP_024308862.1:p.Glu28255Asp
|
|
XM_024453095.1:c.84762G>C
(TTN)
|
XP_024308863.1:p.Glu28254Asp
|
|
XM_024453096.1:c.84195G>C
(TTN)
|
XP_024308864.1:p.Glu28065Asp
|
|
XM_024453097.1:c.81537G>C
(TTN)
|
XP_024308865.1:p.Glu27179Asp
|
|
XM_024453098.1:c.81456G>C
(TTN)
|
XP_024308866.1:p.Glu27152Asp
|
|
XM_024453099.1:c.63219G>C
(TTN)
|
XP_024308867.1:p.Glu21073Asp
|
|
XM_024453100.1:c.53073G>C
(TTN)
|
XP_024308868.1:p.Glu17691Asp
|
|