ENST00000342992.11:c.98293C>G
(TTN)
|
ENSP00000343764.6:p.Gln32765Glu
|
|
ENST00000342175.11:c.79378C>G
(TTN)
|
ENSP00000340554.6:p.Gln26460Glu
|
|
ENST00000359218.10:c.79177C>G
(TTN)
|
ENSP00000352154.5:p.Gln26393Glu
|
|
ENST00000342175.10:c.79378C>G
(TTN)
|
ENSP00000340554.6:p.Gln26460Glu
|
|
ENST00000342992.10:c.98293C>G
(TTN)
|
ENSP00000343764.6:p.Gln32765Glu
|
|
ENST00000359218.9:c.79177C>G
(TTN)
|
ENSP00000352154.5:p.Gln26393Glu
|
|
ENST00000460472.6:c.78802C>G
(TTN)
|
ENSP00000434586.1:p.Gln26268Glu
|
|
ENST00000589042.5:c.105997C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gln35333Glu
|
|
ENST00000591111.5:c.101074C>G
(TTN)
|
ENSP00000465570.1:p.Gln33692Glu
|
|
ENST00000615779.4:c.101074C>G
(TTN)
|
ENSP00000483597.1:p.Gln33692Glu
|
|
NM_001256850.1:c.101074C>G
(TTN)
|
NP_001243779.1:p.Gln33692Glu
|
|
NM_001267550.2:c.105997C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Gln35333Glu
|
|
NM_003319.4:c.78802C>G
(TTN)
|
NP_003310.4:p.Gln26268Glu
|
|
NM_133378.4:c.98293C>G
(TTN)
|
NP_596869.4:p.Gln32765Glu
|
|
NM_133432.3:c.79177C>G
(TTN)
|
NP_597676.3:p.Gln26393Glu
|
|
NM_133437.4:c.79378C>G
(TTN)
|
NP_597681.4:p.Gln26460Glu
|
|
NR_038271.1:n.446+6982G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5114G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105094C>G
(TTN)
|
XP_011510031.1:p.Gln35032Glu
|
|
XM_011511730.1:c.78988C>G
(TTN)
|
XP_011510032.1:p.Gln26330Glu
|
|
XM_011511731.1:c.78847C>G
(TTN)
|
XP_011510033.1:p.Gln26283Glu
|
|
XM_017004819.1:c.104890C>G
(TTN)
|
XP_016860308.1:p.Gln34964Glu
|
|
XM_017004820.1:c.100288C>G
(TTN)
|
XP_016860309.1:p.Gln33430Glu
|
|
XM_017004821.1:c.100285C>G
(TTN)
|
XP_016860310.1:p.Gln33429Glu
|
|
XM_017004822.1:c.97327C>G
(TTN)
|
XP_016860311.1:p.Gln32443Glu
|
|
XM_017004823.1:c.78943C>G
(TTN)
|
XP_016860312.1:p.Gln26315Glu
|
|
XM_024453094.1:c.100438C>G
(TTN)
|
XP_024308862.1:p.Gln33480Glu
|
|
XM_024453095.1:c.100435C>G
(TTN)
|
XP_024308863.1:p.Gln33479Glu
|
|
XM_024453096.1:c.99868C>G
(TTN)
|
XP_024308864.1:p.Gln33290Glu
|
|
XM_024453097.1:c.97210C>G
(TTN)
|
XP_024308865.1:p.Gln32404Glu
|
|
XM_024453098.1:c.97129C>G
(TTN)
|
XP_024308866.1:p.Gln32377Glu
|
|
XM_024453099.1:c.78892C>G
(TTN)
|
XP_024308867.1:p.Gln26298Glu
|
|
XM_024453100.1:c.68746C>G
(TTN)
|
XP_024308868.1:p.Gln22916Glu
|
|