ENST00000342992.11:c.98427A>C
(TTN)
|
ENSP00000343764.6:p.Gln32809His
|
|
ENST00000342175.11:c.79512A>C
(TTN)
|
ENSP00000340554.6:p.Gln26504His
|
|
ENST00000359218.10:c.79311A>C
(TTN)
|
ENSP00000352154.5:p.Gln26437His
|
|
ENST00000342175.10:c.79512A>C
(TTN)
|
ENSP00000340554.6:p.Gln26504His
|
|
ENST00000342992.10:c.98427A>C
(TTN)
|
ENSP00000343764.6:p.Gln32809His
|
|
ENST00000359218.9:c.79311A>C
(TTN)
|
ENSP00000352154.5:p.Gln26437His
|
|
ENST00000460472.6:c.78936A>C
(TTN)
|
ENSP00000434586.1:p.Gln26312His
|
|
ENST00000589042.5:c.106131A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35377His
|
|
ENST00000591111.5:c.101208A>C
(TTN)
|
ENSP00000465570.1:p.Gln33736His
|
|
ENST00000615779.4:c.101208A>C
(TTN)
|
ENSP00000483597.1:p.Gln33736His
|
|
NM_001256850.1:c.101208A>C
(TTN)
|
NP_001243779.1:p.Gln33736His
|
|
NM_001267550.2:c.106131A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35377His
|
|
NM_003319.4:c.78936A>C
(TTN)
|
NP_003310.4:p.Gln26312His
|
|
NM_133378.4:c.98427A>C
(TTN)
|
NP_596869.4:p.Gln32809His
|
|
NM_133432.3:c.79311A>C
(TTN)
|
NP_597676.3:p.Gln26437His
|
|
NM_133437.4:c.79512A>C
(TTN)
|
NP_597681.4:p.Gln26504His
|
|
NR_038271.1:n.446+6848T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5248T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105228A>C
(TTN)
|
XP_011510031.1:p.Gln35076His
|
|
XM_011511730.1:c.79122A>C
(TTN)
|
XP_011510032.1:p.Gln26374His
|
|
XM_011511731.1:c.78981A>C
(TTN)
|
XP_011510033.1:p.Gln26327His
|
|
XM_017004819.1:c.105024A>C
(TTN)
|
XP_016860308.1:p.Gln35008His
|
|
XM_017004820.1:c.100422A>C
(TTN)
|
XP_016860309.1:p.Gln33474His
|
|
XM_017004821.1:c.100419A>C
(TTN)
|
XP_016860310.1:p.Gln33473His
|
|
XM_017004822.1:c.97461A>C
(TTN)
|
XP_016860311.1:p.Gln32487His
|
|
XM_017004823.1:c.79077A>C
(TTN)
|
XP_016860312.1:p.Gln26359His
|
|
XM_024453094.1:c.100572A>C
(TTN)
|
XP_024308862.1:p.Gln33524His
|
|
XM_024453095.1:c.100569A>C
(TTN)
|
XP_024308863.1:p.Gln33523His
|
|
XM_024453096.1:c.100002A>C
(TTN)
|
XP_024308864.1:p.Gln33334His
|
|
XM_024453097.1:c.97344A>C
(TTN)
|
XP_024308865.1:p.Gln32448His
|
|
XM_024453098.1:c.97263A>C
(TTN)
|
XP_024308866.1:p.Gln32421His
|
|
XM_024453099.1:c.79026A>C
(TTN)
|
XP_024308867.1:p.Gln26342His
|
|
XM_024453100.1:c.68880A>C
(TTN)
|
XP_024308868.1:p.Gln22960His
|
|