ENST00000342992.11:c.100182G>A
(TTN)
|
ENSP00000343764.6:p.Gln33394=
|
|
ENST00000342175.11:c.81267G>A
(TTN)
|
ENSP00000340554.6:p.Gln27089=
|
|
ENST00000359218.10:c.81066G>A
(TTN)
|
ENSP00000352154.5:p.Gln27022=
|
|
ENST00000342175.10:c.81267G>A
(TTN)
|
ENSP00000340554.6:p.Gln27089=
|
|
ENST00000342992.10:c.100182G>A
(TTN)
|
ENSP00000343764.6:p.Gln33394=
|
|
ENST00000359218.9:c.81066G>A
(TTN)
|
ENSP00000352154.5:p.Gln27022=
|
|
ENST00000460472.6:c.80691G>A
(TTN)
|
ENSP00000434586.1:p.Gln26897=
|
|
ENST00000589042.5:c.107886G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35962=
|
|
ENST00000591111.5:c.102963G>A
(TTN)
|
ENSP00000465570.1:p.Gln34321=
|
|
ENST00000615779.4:c.102963G>A
(TTN)
|
ENSP00000483597.1:p.Gln34321=
|
|
NM_001256850.1:c.102963G>A
(TTN)
|
NP_001243779.1:p.Gln34321=
|
|
NM_001267550.2:c.107886G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35962=
|
|
NM_003319.4:c.80691G>A
(TTN)
|
NP_003310.4:p.Gln26897=
|
|
NM_133378.4:c.100182G>A
(TTN)
|
NP_596869.4:p.Gln33394=
|
|
NM_133432.3:c.81066G>A
(TTN)
|
NP_597676.3:p.Gln27022=
|
|
NM_133437.4:c.81267G>A
(TTN)
|
NP_597681.4:p.Gln27089=
|
|
NR_038271.1:n.446+3466C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3466C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.106983G>A
(TTN)
|
XP_011510031.1:p.Gln35661=
|
|
XM_011511730.1:c.80877G>A
(TTN)
|
XP_011510032.1:p.Gln26959=
|
|
XM_011511731.1:c.80736G>A
(TTN)
|
XP_011510033.1:p.Gln26912=
|
|
XM_017004819.1:c.106779G>A
(TTN)
|
XP_016860308.1:p.Gln35593=
|
|
XM_017004820.1:c.102177G>A
(TTN)
|
XP_016860309.1:p.Gln34059=
|
|
XM_017004821.1:c.102174G>A
(TTN)
|
XP_016860310.1:p.Gln34058=
|
|
XM_017004822.1:c.99216G>A
(TTN)
|
XP_016860311.1:p.Gln33072=
|
|
XM_017004823.1:c.80832G>A
(TTN)
|
XP_016860312.1:p.Gln26944=
|
|
XM_024453094.1:c.102327G>A
(TTN)
|
XP_024308862.1:p.Gln34109=
|
|
XM_024453095.1:c.102324G>A
(TTN)
|
XP_024308863.1:p.Gln34108=
|
|
XM_024453096.1:c.101757G>A
(TTN)
|
XP_024308864.1:p.Gln33919=
|
|
XM_024453097.1:c.99099G>A
(TTN)
|
XP_024308865.1:p.Gln33033=
|
|
XM_024453098.1:c.99018G>A
(TTN)
|
XP_024308866.1:p.Gln33006=
|
|
XM_024453099.1:c.80781G>A
(TTN)
|
XP_024308867.1:p.Gln26927=
|
|
XM_024453100.1:c.70635G>A
(TTN)
|
XP_024308868.1:p.Gln23545=
|
|