ENST00000342992.11:c.98424G>C
(TTN)
|
ENSP00000343764.6:p.Gly32808=
|
|
ENST00000342175.11:c.79509G>C
(TTN)
|
ENSP00000340554.6:p.Gly26503=
|
|
ENST00000359218.10:c.79308G>C
(TTN)
|
ENSP00000352154.5:p.Gly26436=
|
|
ENST00000342175.10:c.79509G>C
(TTN)
|
ENSP00000340554.6:p.Gly26503=
|
|
ENST00000342992.10:c.98424G>C
(TTN)
|
ENSP00000343764.6:p.Gly32808=
|
|
ENST00000359218.9:c.79308G>C
(TTN)
|
ENSP00000352154.5:p.Gly26436=
|
|
ENST00000460472.6:c.78933G>C
(TTN)
|
ENSP00000434586.1:p.Gly26311=
|
|
ENST00000589042.5:c.106128G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35376=
|
|
ENST00000591111.5:c.101205G>C
(TTN)
|
ENSP00000465570.1:p.Gly33735=
|
|
ENST00000615779.4:c.101205G>C
(TTN)
|
ENSP00000483597.1:p.Gly33735=
|
|
NM_001256850.1:c.101205G>C
(TTN)
|
NP_001243779.1:p.Gly33735=
|
|
NM_001267550.2:c.106128G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35376=
|
|
NM_003319.4:c.78933G>C
(TTN)
|
NP_003310.4:p.Gly26311=
|
|
NM_133378.4:c.98424G>C
(TTN)
|
NP_596869.4:p.Gly32808=
|
|
NM_133432.3:c.79308G>C
(TTN)
|
NP_597676.3:p.Gly26436=
|
|
NM_133437.4:c.79509G>C
(TTN)
|
NP_597681.4:p.Gly26503=
|
|
NR_038271.1:n.446+6851C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5245C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105225G>C
(TTN)
|
XP_011510031.1:p.Gly35075=
|
|
XM_011511730.1:c.79119G>C
(TTN)
|
XP_011510032.1:p.Gly26373=
|
|
XM_011511731.1:c.78978G>C
(TTN)
|
XP_011510033.1:p.Gly26326=
|
|
XM_017004819.1:c.105021G>C
(TTN)
|
XP_016860308.1:p.Gly35007=
|
|
XM_017004820.1:c.100419G>C
(TTN)
|
XP_016860309.1:p.Gly33473=
|
|
XM_017004821.1:c.100416G>C
(TTN)
|
XP_016860310.1:p.Gly33472=
|
|
XM_017004822.1:c.97458G>C
(TTN)
|
XP_016860311.1:p.Gly32486=
|
|
XM_017004823.1:c.79074G>C
(TTN)
|
XP_016860312.1:p.Gly26358=
|
|
XM_024453094.1:c.100569G>C
(TTN)
|
XP_024308862.1:p.Gly33523=
|
|
XM_024453095.1:c.100566G>C
(TTN)
|
XP_024308863.1:p.Gly33522=
|
|
XM_024453096.1:c.99999G>C
(TTN)
|
XP_024308864.1:p.Gly33333=
|
|
XM_024453097.1:c.97341G>C
(TTN)
|
XP_024308865.1:p.Gly32447=
|
|
XM_024453098.1:c.97260G>C
(TTN)
|
XP_024308866.1:p.Gly32420=
|
|
XM_024453099.1:c.79023G>C
(TTN)
|
XP_024308867.1:p.Gly26341=
|
|
XM_024453100.1:c.68877G>C
(TTN)
|
XP_024308868.1:p.Gly22959=
|
|