ENST00000342992.11:c.96714A>G
(TTN)
|
ENSP00000343764.6:p.Gln32238=
|
|
ENST00000342175.11:c.77799A>G
(TTN)
|
ENSP00000340554.6:p.Gln25933=
|
|
ENST00000359218.10:c.77598A>G
(TTN)
|
ENSP00000352154.5:p.Gln25866=
|
|
ENST00000342175.10:c.77799A>G
(TTN)
|
ENSP00000340554.6:p.Gln25933=
|
|
ENST00000342992.10:c.96714A>G
(TTN)
|
ENSP00000343764.6:p.Gln32238=
|
|
ENST00000359218.9:c.77598A>G
(TTN)
|
ENSP00000352154.5:p.Gln25866=
|
|
ENST00000460472.6:c.77223A>G
(TTN)
|
ENSP00000434586.1:p.Gln25741=
|
|
ENST00000589042.5:c.104418A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln34806=
|
|
ENST00000591111.5:c.99495A>G
(TTN)
|
ENSP00000465570.1:p.Gln33165=
|
|
ENST00000615779.4:c.99495A>G
(TTN)
|
ENSP00000483597.1:p.Gln33165=
|
|
NM_001256850.1:c.99495A>G
(TTN)
|
NP_001243779.1:p.Gln33165=
|
|
NM_001267550.2:c.104418A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln34806=
|
|
NM_003319.4:c.77223A>G
(TTN)
|
NP_003310.4:p.Gln25741=
|
|
NM_133378.4:c.96714A>G
(TTN)
|
NP_596869.4:p.Gln32238=
|
|
NM_133432.3:c.77598A>G
(TTN)
|
NP_597676.3:p.Gln25866=
|
|
NM_133437.4:c.77799A>G
(TTN)
|
NP_597681.4:p.Gln25933=
|
|
NR_038271.1:n.446+8561T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3535T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103515A>G
(TTN)
|
XP_011510031.1:p.Gln34505=
|
|
XM_011511730.1:c.77409A>G
(TTN)
|
XP_011510032.1:p.Gln25803=
|
|
XM_011511731.1:c.77268A>G
(TTN)
|
XP_011510033.1:p.Gln25756=
|
|
XM_017004819.1:c.103311A>G
(TTN)
|
XP_016860308.1:p.Gln34437=
|
|
XM_017004820.1:c.98709A>G
(TTN)
|
XP_016860309.1:p.Gln32903=
|
|
XM_017004821.1:c.98706A>G
(TTN)
|
XP_016860310.1:p.Gln32902=
|
|
XM_017004822.1:c.95748A>G
(TTN)
|
XP_016860311.1:p.Gln31916=
|
|
XM_017004823.1:c.77364A>G
(TTN)
|
XP_016860312.1:p.Gln25788=
|
|
XM_024453094.1:c.98859A>G
(TTN)
|
XP_024308862.1:p.Gln32953=
|
|
XM_024453095.1:c.98856A>G
(TTN)
|
XP_024308863.1:p.Gln32952=
|
|
XM_024453096.1:c.98289A>G
(TTN)
|
XP_024308864.1:p.Gln32763=
|
|
XM_024453097.1:c.95631A>G
(TTN)
|
XP_024308865.1:p.Gln31877=
|
|
XM_024453098.1:c.95550A>G
(TTN)
|
XP_024308866.1:p.Gln31850=
|
|
XM_024453099.1:c.77313A>G
(TTN)
|
XP_024308867.1:p.Gln25771=
|
|
XM_024453100.1:c.67167A>G
(TTN)
|
XP_024308868.1:p.Gln22389=
|
|