ENST00000342992.11:c.52899A>T
(TTN)
|
ENSP00000343764.6:p.Gly17633=
|
|
ENST00000342175.11:c.33984A>T
(TTN)
|
ENSP00000340554.6:p.Gly11328=
|
|
ENST00000359218.10:c.33783A>T
(TTN)
|
ENSP00000352154.5:p.Gly11261=
|
|
ENST00000342175.10:c.33984A>T
(TTN)
|
ENSP00000340554.6:p.Gly11328=
|
|
ENST00000342992.10:c.52899A>T
(TTN)
|
ENSP00000343764.6:p.Gly17633=
|
|
ENST00000359218.9:c.33783A>T
(TTN)
|
ENSP00000352154.5:p.Gly11261=
|
|
ENST00000460472.6:c.33408A>T
(TTN)
|
ENSP00000434586.1:p.Gly11136=
|
|
ENST00000589042.5:c.60603A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly20201=
|
|
ENST00000591111.5:c.55680A>T
(TTN)
|
ENSP00000465570.1:p.Gly18560=
|
|
ENST00000615779.4:c.55680A>T
(TTN)
|
ENSP00000483597.1:p.Gly18560=
|
|
NM_001256850.1:c.55680A>T
(TTN)
|
NP_001243779.1:p.Gly18560=
|
|
NM_001267550.2:c.60603A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly20201=
|
|
NM_003319.4:c.33408A>T
(TTN)
|
NP_003310.4:p.Gly11136=
|
|
NM_133378.4:c.52899A>T
(TTN)
|
NP_596869.4:p.Gly17633=
|
|
NM_133432.3:c.33783A>T
(TTN)
|
NP_597676.3:p.Gly11261=
|
|
NM_133437.4:c.33984A>T
(TTN)
|
NP_597681.4:p.Gly11328=
|
|
NR_038271.1:n.597-6474T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-17T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59700A>T
(TTN)
|
XP_011510031.1:p.Gly19900=
|
|
XM_011511730.1:c.33594A>T
(TTN)
|
XP_011510032.1:p.Gly11198=
|
|
XM_011511731.1:c.33453A>T
(TTN)
|
XP_011510033.1:p.Gly11151=
|
|
XM_017004819.1:c.59496A>T
(TTN)
|
XP_016860308.1:p.Gly19832=
|
|
XM_017004820.1:c.54894A>T
(TTN)
|
XP_016860309.1:p.Gly18298=
|
|
XM_017004821.1:c.54891A>T
(TTN)
|
XP_016860310.1:p.Gly18297=
|
|
XM_017004822.1:c.51933A>T
(TTN)
|
XP_016860311.1:p.Gly17311=
|
|
XM_017004823.1:c.33549A>T
(TTN)
|
XP_016860312.1:p.Gly11183=
|
|
XM_024453094.1:c.55044A>T
(TTN)
|
XP_024308862.1:p.Gly18348=
|
|
XM_024453095.1:c.55041A>T
(TTN)
|
XP_024308863.1:p.Gly18347=
|
|
XM_024453096.1:c.54474A>T
(TTN)
|
XP_024308864.1:p.Gly18158=
|
|
XM_024453097.1:c.51816A>T
(TTN)
|
XP_024308865.1:p.Gly17272=
|
|
XM_024453098.1:c.51735A>T
(TTN)
|
XP_024308866.1:p.Gly17245=
|
|
XM_024453099.1:c.33498A>T
(TTN)
|
XP_024308867.1:p.Gly11166=
|
|
XM_024453100.1:c.23352A>T
(TTN)
|
XP_024308868.1:p.Gly7784=
|
|