ENST00000342992.11:c.99897T>G
(TTN)
|
ENSP00000343764.6:p.Ser33299Arg
|
|
ENST00000342175.11:c.80982T>G
(TTN)
|
ENSP00000340554.6:p.Ser26994Arg
|
|
ENST00000359218.10:c.80781T>G
(TTN)
|
ENSP00000352154.5:p.Ser26927Arg
|
|
ENST00000342175.10:c.80982T>G
(TTN)
|
ENSP00000340554.6:p.Ser26994Arg
|
|
ENST00000342992.10:c.99897T>G
(TTN)
|
ENSP00000343764.6:p.Ser33299Arg
|
|
ENST00000359218.9:c.80781T>G
(TTN)
|
ENSP00000352154.5:p.Ser26927Arg
|
|
ENST00000460472.6:c.80406T>G
(TTN)
|
ENSP00000434586.1:p.Ser26802Arg
|
|
ENST00000589042.5:c.107601T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35867Arg
|
|
ENST00000591111.5:c.102678T>G
(TTN)
|
ENSP00000465570.1:p.Ser34226Arg
|
|
ENST00000615779.4:c.102678T>G
(TTN)
|
ENSP00000483597.1:p.Ser34226Arg
|
|
NM_001256850.1:c.102678T>G
(TTN)
|
NP_001243779.1:p.Ser34226Arg
|
|
NM_001267550.2:c.107601T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35867Arg
|
|
NM_003319.4:c.80406T>G
(TTN)
|
NP_003310.4:p.Ser26802Arg
|
|
NM_133378.4:c.99897T>G
(TTN)
|
NP_596869.4:p.Ser33299Arg
|
|
NM_133432.3:c.80781T>G
(TTN)
|
NP_597676.3:p.Ser26927Arg
|
|
NM_133437.4:c.80982T>G
(TTN)
|
NP_597681.4:p.Ser26994Arg
|
|
NR_038271.1:n.446+3889A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3889A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.106698T>G
(TTN)
|
XP_011510031.1:p.Ser35566Arg
|
|
XM_011511730.1:c.80592T>G
(TTN)
|
XP_011510032.1:p.Ser26864Arg
|
|
XM_011511731.1:c.80451T>G
(TTN)
|
XP_011510033.1:p.Ser26817Arg
|
|
XM_017004819.1:c.106494T>G
(TTN)
|
XP_016860308.1:p.Ser35498Arg
|
|
XM_017004820.1:c.101892T>G
(TTN)
|
XP_016860309.1:p.Ser33964Arg
|
|
XM_017004821.1:c.101889T>G
(TTN)
|
XP_016860310.1:p.Ser33963Arg
|
|
XM_017004822.1:c.98931T>G
(TTN)
|
XP_016860311.1:p.Ser32977Arg
|
|
XM_017004823.1:c.80547T>G
(TTN)
|
XP_016860312.1:p.Ser26849Arg
|
|
XM_024453094.1:c.102042T>G
(TTN)
|
XP_024308862.1:p.Ser34014Arg
|
|
XM_024453095.1:c.102039T>G
(TTN)
|
XP_024308863.1:p.Ser34013Arg
|
|
XM_024453096.1:c.101472T>G
(TTN)
|
XP_024308864.1:p.Ser33824Arg
|
|
XM_024453097.1:c.98814T>G
(TTN)
|
XP_024308865.1:p.Ser32938Arg
|
|
XM_024453098.1:c.98733T>G
(TTN)
|
XP_024308866.1:p.Ser32911Arg
|
|
XM_024453099.1:c.80496T>G
(TTN)
|
XP_024308867.1:p.Ser26832Arg
|
|
XM_024453100.1:c.70350T>G
(TTN)
|
XP_024308868.1:p.Ser23450Arg
|
|