ENST00000342992.11:c.83761G>T
(TTN)
|
ENSP00000343764.6:p.Gly27921Trp
|
|
ENST00000342175.11:c.64846G>T
(TTN)
|
ENSP00000340554.6:p.Gly21616Trp
|
|
ENST00000359218.10:c.64645G>T
(TTN)
|
ENSP00000352154.5:p.Gly21549Trp
|
|
ENST00000342175.10:c.64846G>T
(TTN)
|
ENSP00000340554.6:p.Gly21616Trp
|
|
ENST00000342992.10:c.83761G>T
(TTN)
|
ENSP00000343764.6:p.Gly27921Trp
|
|
ENST00000359218.9:c.64645G>T
(TTN)
|
ENSP00000352154.5:p.Gly21549Trp
|
|
ENST00000460472.6:c.64270G>T
(TTN)
|
ENSP00000434586.1:p.Gly21424Trp
|
|
ENST00000589042.5:c.91465G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30489Trp
|
|
ENST00000591111.5:c.86542G>T
(TTN)
|
ENSP00000465570.1:p.Gly28848Trp
|
|
ENST00000615779.4:c.86542G>T
(TTN)
|
ENSP00000483597.1:p.Gly28848Trp
|
|
NM_001256850.1:c.86542G>T
(TTN)
|
NP_001243779.1:p.Gly28848Trp
|
|
NM_001267550.2:c.91465G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30489Trp
|
|
NM_003319.4:c.64270G>T
(TTN)
|
NP_003310.4:p.Gly21424Trp
|
|
NM_133378.4:c.83761G>T
(TTN)
|
NP_596869.4:p.Gly27921Trp
|
|
NM_133432.3:c.64645G>T
(TTN)
|
NP_597676.3:p.Gly21549Trp
|
|
NM_133437.4:c.64846G>T
(TTN)
|
NP_597681.4:p.Gly21616Trp
|
|
NR_038271.1:n.447-20234C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+8705C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.90562G>T
(TTN)
|
XP_011510031.1:p.Gly30188Trp
|
|
XM_011511730.1:c.64456G>T
(TTN)
|
XP_011510032.1:p.Gly21486Trp
|
|
XM_011511731.1:c.64315G>T
(TTN)
|
XP_011510033.1:p.Gly21439Trp
|
|
XM_017004819.1:c.90358G>T
(TTN)
|
XP_016860308.1:p.Gly30120Trp
|
|
XM_017004820.1:c.85756G>T
(TTN)
|
XP_016860309.1:p.Gly28586Trp
|
|
XM_017004821.1:c.85753G>T
(TTN)
|
XP_016860310.1:p.Gly28585Trp
|
|
XM_017004822.1:c.82795G>T
(TTN)
|
XP_016860311.1:p.Gly27599Trp
|
|
XM_017004823.1:c.64411G>T
(TTN)
|
XP_016860312.1:p.Gly21471Trp
|
|
XM_024453094.1:c.85906G>T
(TTN)
|
XP_024308862.1:p.Gly28636Trp
|
|
XM_024453095.1:c.85903G>T
(TTN)
|
XP_024308863.1:p.Gly28635Trp
|
|
XM_024453096.1:c.85336G>T
(TTN)
|
XP_024308864.1:p.Gly28446Trp
|
|
XM_024453097.1:c.82678G>T
(TTN)
|
XP_024308865.1:p.Gly27560Trp
|
|
XM_024453098.1:c.82597G>T
(TTN)
|
XP_024308866.1:p.Gly27533Trp
|
|
XM_024453099.1:c.64360G>T
(TTN)
|
XP_024308867.1:p.Gly21454Trp
|
|
XM_024453100.1:c.54214G>T
(TTN)
|
XP_024308868.1:p.Gly18072Trp
|
|