ENST00000342992.11:c.98682A>G
(TTN)
|
ENSP00000343764.6:p.Gln32894=
|
|
ENST00000342175.11:c.79767A>G
(TTN)
|
ENSP00000340554.6:p.Gln26589=
|
|
ENST00000359218.10:c.79566A>G
(TTN)
|
ENSP00000352154.5:p.Gln26522=
|
|
ENST00000342175.10:c.79767A>G
(TTN)
|
ENSP00000340554.6:p.Gln26589=
|
|
ENST00000342992.10:c.98682A>G
(TTN)
|
ENSP00000343764.6:p.Gln32894=
|
|
ENST00000359218.9:c.79566A>G
(TTN)
|
ENSP00000352154.5:p.Gln26522=
|
|
ENST00000460472.6:c.79191A>G
(TTN)
|
ENSP00000434586.1:p.Gln26397=
|
|
ENST00000589042.5:c.106386A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35462=
|
|
ENST00000591111.5:c.101463A>G
(TTN)
|
ENSP00000465570.1:p.Gln33821=
|
|
ENST00000615779.4:c.101463A>G
(TTN)
|
ENSP00000483597.1:p.Gln33821=
|
|
NM_001256850.1:c.101463A>G
(TTN)
|
NP_001243779.1:p.Gln33821=
|
|
NM_001267550.2:c.106386A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35462=
|
|
NM_003319.4:c.79191A>G
(TTN)
|
NP_003310.4:p.Gln26397=
|
|
NM_133378.4:c.98682A>G
(TTN)
|
NP_596869.4:p.Gln32894=
|
|
NM_133432.3:c.79566A>G
(TTN)
|
NP_597676.3:p.Gln26522=
|
|
NM_133437.4:c.79767A>G
(TTN)
|
NP_597681.4:p.Gln26589=
|
|
NR_038271.1:n.446+6469T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5627T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105483A>G
(TTN)
|
XP_011510031.1:p.Gln35161=
|
|
XM_011511730.1:c.79377A>G
(TTN)
|
XP_011510032.1:p.Gln26459=
|
|
XM_011511731.1:c.79236A>G
(TTN)
|
XP_011510033.1:p.Gln26412=
|
|
XM_017004819.1:c.105279A>G
(TTN)
|
XP_016860308.1:p.Gln35093=
|
|
XM_017004820.1:c.100677A>G
(TTN)
|
XP_016860309.1:p.Gln33559=
|
|
XM_017004821.1:c.100674A>G
(TTN)
|
XP_016860310.1:p.Gln33558=
|
|
XM_017004822.1:c.97716A>G
(TTN)
|
XP_016860311.1:p.Gln32572=
|
|
XM_017004823.1:c.79332A>G
(TTN)
|
XP_016860312.1:p.Gln26444=
|
|
XM_024453094.1:c.100827A>G
(TTN)
|
XP_024308862.1:p.Gln33609=
|
|
XM_024453095.1:c.100824A>G
(TTN)
|
XP_024308863.1:p.Gln33608=
|
|
XM_024453096.1:c.100257A>G
(TTN)
|
XP_024308864.1:p.Gln33419=
|
|
XM_024453097.1:c.97599A>G
(TTN)
|
XP_024308865.1:p.Gln32533=
|
|
XM_024453098.1:c.97518A>G
(TTN)
|
XP_024308866.1:p.Gln32506=
|
|
XM_024453099.1:c.79281A>G
(TTN)
|
XP_024308867.1:p.Gln26427=
|
|
XM_024453100.1:c.69135A>G
(TTN)
|
XP_024308868.1:p.Gln23045=
|
|