ENST00000342992.11:c.92333T>C
(TTN)
|
ENSP00000343764.6:p.Ile30778Thr
|
|
ENST00000342175.11:c.73418T>C
(TTN)
|
ENSP00000340554.6:p.Ile24473Thr
|
|
ENST00000359218.10:c.73217T>C
(TTN)
|
ENSP00000352154.5:p.Ile24406Thr
|
|
ENST00000342175.10:c.73418T>C
(TTN)
|
ENSP00000340554.6:p.Ile24473Thr
|
|
ENST00000342992.10:c.92333T>C
(TTN)
|
ENSP00000343764.6:p.Ile30778Thr
|
|
ENST00000359218.9:c.73217T>C
(TTN)
|
ENSP00000352154.5:p.Ile24406Thr
|
|
ENST00000460472.6:c.72842T>C
(TTN)
|
ENSP00000434586.1:p.Ile24281Thr
|
|
ENST00000589042.5:c.100037T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile33346Thr
|
|
ENST00000591111.5:c.95114T>C
(TTN)
|
ENSP00000465570.1:p.Ile31705Thr
|
|
ENST00000615779.4:c.95114T>C
(TTN)
|
ENSP00000483597.1:p.Ile31705Thr
|
|
NM_001256850.1:c.95114T>C
(TTN)
|
NP_001243779.1:p.Ile31705Thr
|
|
NM_001267550.2:c.100037T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ile33346Thr
|
|
NM_003319.4:c.72842T>C
(TTN)
|
NP_003310.4:p.Ile24281Thr
|
|
NM_133378.4:c.92333T>C
(TTN)
|
NP_596869.4:p.Ile30778Thr
|
|
NM_133432.3:c.73217T>C
(TTN)
|
NP_597676.3:p.Ile24406Thr
|
|
NM_133437.4:c.73418T>C
(TTN)
|
NP_597681.4:p.Ile24473Thr
|
|
NR_038271.1:n.446+13436A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.317-289A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.99134T>C
(TTN)
|
XP_011510031.1:p.Ile33045Thr
|
|
XM_011511730.1:c.73028T>C
(TTN)
|
XP_011510032.1:p.Ile24343Thr
|
|
XM_011511731.1:c.72887T>C
(TTN)
|
XP_011510033.1:p.Ile24296Thr
|
|
XM_017004819.1:c.98930T>C
(TTN)
|
XP_016860308.1:p.Ile32977Thr
|
|
XM_017004820.1:c.94328T>C
(TTN)
|
XP_016860309.1:p.Ile31443Thr
|
|
XM_017004821.1:c.94325T>C
(TTN)
|
XP_016860310.1:p.Ile31442Thr
|
|
XM_017004822.1:c.91367T>C
(TTN)
|
XP_016860311.1:p.Ile30456Thr
|
|
XM_017004823.1:c.72983T>C
(TTN)
|
XP_016860312.1:p.Ile24328Thr
|
|
XM_024453094.1:c.94478T>C
(TTN)
|
XP_024308862.1:p.Ile31493Thr
|
|
XM_024453095.1:c.94475T>C
(TTN)
|
XP_024308863.1:p.Ile31492Thr
|
|
XM_024453096.1:c.93908T>C
(TTN)
|
XP_024308864.1:p.Ile31303Thr
|
|
XM_024453097.1:c.91250T>C
(TTN)
|
XP_024308865.1:p.Ile30417Thr
|
|
XM_024453098.1:c.91169T>C
(TTN)
|
XP_024308866.1:p.Ile30390Thr
|
|
XM_024453099.1:c.72932T>C
(TTN)
|
XP_024308867.1:p.Ile24311Thr
|
|
XM_024453100.1:c.62786T>C
(TTN)
|
XP_024308868.1:p.Ile20929Thr
|
|