ENST00000342992.11:c.54708C>G
(TTN)
|
ENSP00000343764.6:p.Thr18236=
|
|
ENST00000342175.11:c.35793C>G
(TTN)
|
ENSP00000340554.6:p.Thr11931=
|
|
ENST00000359218.10:c.35592C>G
(TTN)
|
ENSP00000352154.5:p.Thr11864=
|
|
ENST00000342175.10:c.35793C>G
(TTN)
|
ENSP00000340554.6:p.Thr11931=
|
|
ENST00000342992.10:c.54708C>G
(TTN)
|
ENSP00000343764.6:p.Thr18236=
|
|
ENST00000359218.9:c.35592C>G
(TTN)
|
ENSP00000352154.5:p.Thr11864=
|
|
ENST00000460472.6:c.35217C>G
(TTN)
|
ENSP00000434586.1:p.Thr11739=
|
|
ENST00000589042.5:c.62412C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr20804=
|
|
ENST00000591111.5:c.57489C>G
(TTN)
|
ENSP00000465570.1:p.Thr19163=
|
|
ENST00000615779.4:c.57489C>G
(TTN)
|
ENSP00000483597.1:p.Thr19163=
|
|
NM_001256850.1:c.57489C>G
(TTN)
|
NP_001243779.1:p.Thr19163=
|
|
NM_001267550.2:c.62412C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr20804=
|
|
NM_003319.4:c.35217C>G
(TTN)
|
NP_003310.4:p.Thr11739=
|
|
NM_133378.4:c.54708C>G
(TTN)
|
NP_596869.4:p.Thr18236=
|
|
NM_133432.3:c.35592C>G
(TTN)
|
NP_597676.3:p.Thr11864=
|
|
NM_133437.4:c.35793C>G
(TTN)
|
NP_597681.4:p.Thr11931=
|
|
NR_038271.1:n.597-8283G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-1826G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.61509C>G
(TTN)
|
XP_011510031.1:p.Thr20503=
|
|
XM_011511730.1:c.35403C>G
(TTN)
|
XP_011510032.1:p.Thr11801=
|
|
XM_011511731.1:c.35262C>G
(TTN)
|
XP_011510033.1:p.Thr11754=
|
|
XM_017004819.1:c.61305C>G
(TTN)
|
XP_016860308.1:p.Thr20435=
|
|
XM_017004820.1:c.56703C>G
(TTN)
|
XP_016860309.1:p.Thr18901=
|
|
XM_017004821.1:c.56700C>G
(TTN)
|
XP_016860310.1:p.Thr18900=
|
|
XM_017004822.1:c.53742C>G
(TTN)
|
XP_016860311.1:p.Thr17914=
|
|
XM_017004823.1:c.35358C>G
(TTN)
|
XP_016860312.1:p.Thr11786=
|
|
XM_024453094.1:c.56853C>G
(TTN)
|
XP_024308862.1:p.Thr18951=
|
|
XM_024453095.1:c.56850C>G
(TTN)
|
XP_024308863.1:p.Thr18950=
|
|
XM_024453096.1:c.56283C>G
(TTN)
|
XP_024308864.1:p.Thr18761=
|
|
XM_024453097.1:c.53625C>G
(TTN)
|
XP_024308865.1:p.Thr17875=
|
|
XM_024453098.1:c.53544C>G
(TTN)
|
XP_024308866.1:p.Thr17848=
|
|
XM_024453099.1:c.35307C>G
(TTN)
|
XP_024308867.1:p.Thr11769=
|
|
XM_024453100.1:c.25161C>G
(TTN)
|
XP_024308868.1:p.Thr8387=
|
|