ENST00000342992.11:c.73822C>G
(TTN)
|
ENSP00000343764.6:p.Arg24608Gly
|
|
ENST00000342175.11:c.54907C>G
(TTN)
|
ENSP00000340554.6:p.Arg18303Gly
|
|
ENST00000359218.10:c.54706C>G
(TTN)
|
ENSP00000352154.5:p.Arg18236Gly
|
|
ENST00000342175.10:c.54907C>G
(TTN)
|
ENSP00000340554.6:p.Arg18303Gly
|
|
ENST00000342992.10:c.73822C>G
(TTN)
|
ENSP00000343764.6:p.Arg24608Gly
|
|
ENST00000359218.9:c.54706C>G
(TTN)
|
ENSP00000352154.5:p.Arg18236Gly
|
|
ENST00000460472.6:c.54331C>G
(TTN)
|
ENSP00000434586.1:p.Arg18111Gly
|
|
ENST00000589042.5:c.81526C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg27176Gly
|
|
ENST00000591111.5:c.76603C>G
(TTN)
|
ENSP00000465570.1:p.Arg25535Gly
|
|
ENST00000615779.4:c.76603C>G
(TTN)
|
ENSP00000483597.1:p.Arg25535Gly
|
|
NM_001256850.1:c.76603C>G
(TTN)
|
NP_001243779.1:p.Arg25535Gly
|
|
NM_001267550.2:c.81526C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg27176Gly
|
|
NM_003319.4:c.54331C>G
(TTN)
|
NP_003310.4:p.Arg18111Gly
|
|
NM_133378.4:c.73822C>G
(TTN)
|
NP_596869.4:p.Arg24608Gly
|
|
NM_133432.3:c.54706C>G
(TTN)
|
NP_597676.3:p.Arg18236Gly
|
|
NM_133437.4:c.54907C>G
(TTN)
|
NP_597681.4:p.Arg18303Gly
|
|
NR_038271.1:n.447-6694G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-17966G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.80623C>G
(TTN)
|
XP_011510031.1:p.Arg26875Gly
|
|
XM_011511730.1:c.54517C>G
(TTN)
|
XP_011510032.1:p.Arg18173Gly
|
|
XM_011511731.1:c.54376C>G
(TTN)
|
XP_011510033.1:p.Arg18126Gly
|
|
XM_017004819.1:c.80419C>G
(TTN)
|
XP_016860308.1:p.Arg26807Gly
|
|
XM_017004820.1:c.75817C>G
(TTN)
|
XP_016860309.1:p.Arg25273Gly
|
|
XM_017004821.1:c.75814C>G
(TTN)
|
XP_016860310.1:p.Arg25272Gly
|
|
XM_017004822.1:c.72856C>G
(TTN)
|
XP_016860311.1:p.Arg24286Gly
|
|
XM_017004823.1:c.54472C>G
(TTN)
|
XP_016860312.1:p.Arg18158Gly
|
|
XM_024453094.1:c.75967C>G
(TTN)
|
XP_024308862.1:p.Arg25323Gly
|
|
XM_024453095.1:c.75964C>G
(TTN)
|
XP_024308863.1:p.Arg25322Gly
|
|
XM_024453096.1:c.75397C>G
(TTN)
|
XP_024308864.1:p.Arg25133Gly
|
|
XM_024453097.1:c.72739C>G
(TTN)
|
XP_024308865.1:p.Arg24247Gly
|
|
XM_024453098.1:c.72658C>G
(TTN)
|
XP_024308866.1:p.Arg24220Gly
|
|
XM_024453099.1:c.54421C>G
(TTN)
|
XP_024308867.1:p.Arg18141Gly
|
|
XM_024453100.1:c.44275C>G
(TTN)
|
XP_024308868.1:p.Arg14759Gly
|
|