ENST00000342992.11:c.73918G>T
(TTN)
|
ENSP00000343764.6:p.Glu24640Ter
|
|
ENST00000342175.11:c.55003G>T
(TTN)
|
ENSP00000340554.6:p.Glu18335Ter
|
|
ENST00000359218.10:c.54802G>T
(TTN)
|
ENSP00000352154.5:p.Glu18268Ter
|
|
ENST00000342175.10:c.55003G>T
(TTN)
|
ENSP00000340554.6:p.Glu18335Ter
|
|
ENST00000342992.10:c.73918G>T
(TTN)
|
ENSP00000343764.6:p.Glu24640Ter
|
|
ENST00000359218.9:c.54802G>T
(TTN)
|
ENSP00000352154.5:p.Glu18268Ter
|
|
ENST00000460472.6:c.54427G>T
(TTN)
|
ENSP00000434586.1:p.Glu18143Ter
|
|
ENST00000589042.5:c.81622G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu27208Ter
|
|
ENST00000591111.5:c.76699G>T
(TTN)
|
ENSP00000465570.1:p.Glu25567Ter
|
|
ENST00000615779.4:c.76699G>T
(TTN)
|
ENSP00000483597.1:p.Glu25567Ter
|
|
NM_001256850.1:c.76699G>T
(TTN)
|
NP_001243779.1:p.Glu25567Ter
|
|
NM_001267550.2:c.81622G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu27208Ter
|
|
NM_003319.4:c.54427G>T
(TTN)
|
NP_003310.4:p.Glu18143Ter
|
|
NM_133378.4:c.73918G>T
(TTN)
|
NP_596869.4:p.Glu24640Ter
|
|
NM_133432.3:c.54802G>T
(TTN)
|
NP_597676.3:p.Glu18268Ter
|
|
NM_133437.4:c.55003G>T
(TTN)
|
NP_597681.4:p.Glu18335Ter
|
|
NR_038271.1:n.447-6790C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-18062C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.80719G>T
(TTN)
|
XP_011510031.1:p.Glu26907Ter
|
|
XM_011511730.1:c.54613G>T
(TTN)
|
XP_011510032.1:p.Glu18205Ter
|
|
XM_011511731.1:c.54472G>T
(TTN)
|
XP_011510033.1:p.Glu18158Ter
|
|
XM_017004819.1:c.80515G>T
(TTN)
|
XP_016860308.1:p.Glu26839Ter
|
|
XM_017004820.1:c.75913G>T
(TTN)
|
XP_016860309.1:p.Glu25305Ter
|
|
XM_017004821.1:c.75910G>T
(TTN)
|
XP_016860310.1:p.Glu25304Ter
|
|
XM_017004822.1:c.72952G>T
(TTN)
|
XP_016860311.1:p.Glu24318Ter
|
|
XM_017004823.1:c.54568G>T
(TTN)
|
XP_016860312.1:p.Glu18190Ter
|
|
XM_024453094.1:c.76063G>T
(TTN)
|
XP_024308862.1:p.Glu25355Ter
|
|
XM_024453095.1:c.76060G>T
(TTN)
|
XP_024308863.1:p.Glu25354Ter
|
|
XM_024453096.1:c.75493G>T
(TTN)
|
XP_024308864.1:p.Glu25165Ter
|
|
XM_024453097.1:c.72835G>T
(TTN)
|
XP_024308865.1:p.Glu24279Ter
|
|
XM_024453098.1:c.72754G>T
(TTN)
|
XP_024308866.1:p.Glu24252Ter
|
|
XM_024453099.1:c.54517G>T
(TTN)
|
XP_024308867.1:p.Glu18173Ter
|
|
XM_024453100.1:c.44371G>T
(TTN)
|
XP_024308868.1:p.Glu14791Ter
|
|