ENST00000342992.11:c.69606A>G
(TTN)
|
ENSP00000343764.6:p.Arg23202=
|
|
ENST00000342175.11:c.50691A>G
(TTN)
|
ENSP00000340554.6:p.Arg16897=
|
|
ENST00000359218.10:c.50490A>G
(TTN)
|
ENSP00000352154.5:p.Arg16830=
|
|
ENST00000342175.10:c.50691A>G
(TTN)
|
ENSP00000340554.6:p.Arg16897=
|
|
ENST00000342992.10:c.69606A>G
(TTN)
|
ENSP00000343764.6:p.Arg23202=
|
|
ENST00000359218.9:c.50490A>G
(TTN)
|
ENSP00000352154.5:p.Arg16830=
|
|
ENST00000460472.6:c.50115A>G
(TTN)
|
ENSP00000434586.1:p.Arg16705=
|
|
ENST00000589042.5:c.77310A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg25770=
|
|
ENST00000591111.5:c.72387A>G
(TTN)
|
ENSP00000465570.1:p.Arg24129=
|
|
ENST00000615779.4:c.72387A>G
(TTN)
|
ENSP00000483597.1:p.Arg24129=
|
|
NM_001256850.1:c.72387A>G
(TTN)
|
NP_001243779.1:p.Arg24129=
|
|
NM_001267550.2:c.77310A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg25770=
|
|
NM_003319.4:c.50115A>G
(TTN)
|
NP_003310.4:p.Arg16705=
|
|
NM_133378.4:c.69606A>G
(TTN)
|
NP_596869.4:p.Arg23202=
|
|
NM_133432.3:c.50490A>G
(TTN)
|
NP_597676.3:p.Arg16830=
|
|
NM_133437.4:c.50691A>G
(TTN)
|
NP_597681.4:p.Arg16897=
|
|
NR_038271.1:n.447-2478T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13750T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76407A>G
(TTN)
|
XP_011510031.1:p.Arg25469=
|
|
XM_011511730.1:c.50301A>G
(TTN)
|
XP_011510032.1:p.Arg16767=
|
|
XM_011511731.1:c.50160A>G
(TTN)
|
XP_011510033.1:p.Arg16720=
|
|
XM_017004819.1:c.76203A>G
(TTN)
|
XP_016860308.1:p.Arg25401=
|
|
XM_017004820.1:c.71601A>G
(TTN)
|
XP_016860309.1:p.Arg23867=
|
|
XM_017004821.1:c.71598A>G
(TTN)
|
XP_016860310.1:p.Arg23866=
|
|
XM_017004822.1:c.68640A>G
(TTN)
|
XP_016860311.1:p.Arg22880=
|
|
XM_017004823.1:c.50256A>G
(TTN)
|
XP_016860312.1:p.Arg16752=
|
|
XM_024453094.1:c.71751A>G
(TTN)
|
XP_024308862.1:p.Arg23917=
|
|
XM_024453095.1:c.71748A>G
(TTN)
|
XP_024308863.1:p.Arg23916=
|
|
XM_024453096.1:c.71181A>G
(TTN)
|
XP_024308864.1:p.Arg23727=
|
|
XM_024453097.1:c.68523A>G
(TTN)
|
XP_024308865.1:p.Arg22841=
|
|
XM_024453098.1:c.68442A>G
(TTN)
|
XP_024308866.1:p.Arg22814=
|
|
XM_024453099.1:c.50205A>G
(TTN)
|
XP_024308867.1:p.Arg16735=
|
|
XM_024453100.1:c.40059A>G
(TTN)
|
XP_024308868.1:p.Arg13353=
|
|