ENST00000342992.11:c.54610G>C
(TTN)
|
ENSP00000343764.6:p.Asp18204His
|
|
ENST00000342175.11:c.35695G>C
(TTN)
|
ENSP00000340554.6:p.Asp11899His
|
|
ENST00000359218.10:c.35494G>C
(TTN)
|
ENSP00000352154.5:p.Asp11832His
|
|
ENST00000342175.10:c.35695G>C
(TTN)
|
ENSP00000340554.6:p.Asp11899His
|
|
ENST00000342992.10:c.54610G>C
(TTN)
|
ENSP00000343764.6:p.Asp18204His
|
|
ENST00000359218.9:c.35494G>C
(TTN)
|
ENSP00000352154.5:p.Asp11832His
|
|
ENST00000460472.6:c.35119G>C
(TTN)
|
ENSP00000434586.1:p.Asp11707His
|
|
ENST00000589042.5:c.62314G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp20772His
|
|
ENST00000591111.5:c.57391G>C
(TTN)
|
ENSP00000465570.1:p.Asp19131His
|
|
ENST00000615779.4:c.57391G>C
(TTN)
|
ENSP00000483597.1:p.Asp19131His
|
|
NM_001256850.1:c.57391G>C
(TTN)
|
NP_001243779.1:p.Asp19131His
|
|
NM_001267550.2:c.62314G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp20772His
|
|
NM_003319.4:c.35119G>C
(TTN)
|
NP_003310.4:p.Asp11707His
|
|
NM_133378.4:c.54610G>C
(TTN)
|
NP_596869.4:p.Asp18204His
|
|
NM_133432.3:c.35494G>C
(TTN)
|
NP_597676.3:p.Asp11832His
|
|
NM_133437.4:c.35695G>C
(TTN)
|
NP_597681.4:p.Asp11899His
|
|
NR_038271.1:n.597-8185C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-1728C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.61411G>C
(TTN)
|
XP_011510031.1:p.Asp20471His
|
|
XM_011511730.1:c.35305G>C
(TTN)
|
XP_011510032.1:p.Asp11769His
|
|
XM_011511731.1:c.35164G>C
(TTN)
|
XP_011510033.1:p.Asp11722His
|
|
XM_017004819.1:c.61207G>C
(TTN)
|
XP_016860308.1:p.Asp20403His
|
|
XM_017004820.1:c.56605G>C
(TTN)
|
XP_016860309.1:p.Asp18869His
|
|
XM_017004821.1:c.56602G>C
(TTN)
|
XP_016860310.1:p.Asp18868His
|
|
XM_017004822.1:c.53644G>C
(TTN)
|
XP_016860311.1:p.Asp17882His
|
|
XM_017004823.1:c.35260G>C
(TTN)
|
XP_016860312.1:p.Asp11754His
|
|
XM_024453094.1:c.56755G>C
(TTN)
|
XP_024308862.1:p.Asp18919His
|
|
XM_024453095.1:c.56752G>C
(TTN)
|
XP_024308863.1:p.Asp18918His
|
|
XM_024453096.1:c.56185G>C
(TTN)
|
XP_024308864.1:p.Asp18729His
|
|
XM_024453097.1:c.53527G>C
(TTN)
|
XP_024308865.1:p.Asp17843His
|
|
XM_024453098.1:c.53446G>C
(TTN)
|
XP_024308866.1:p.Asp17816His
|
|
XM_024453099.1:c.35209G>C
(TTN)
|
XP_024308867.1:p.Asp11737His
|
|
XM_024453100.1:c.25063G>C
(TTN)
|
XP_024308868.1:p.Asp8355His
|
|