ENST00000342992.11:c.87111C>A
(TTN)
|
ENSP00000343764.6:p.Cys29037Ter
|
|
ENST00000342175.11:c.68196C>A
(TTN)
|
ENSP00000340554.6:p.Cys22732Ter
|
|
ENST00000359218.10:c.67995C>A
(TTN)
|
ENSP00000352154.5:p.Cys22665Ter
|
|
ENST00000342175.10:c.68196C>A
(TTN)
|
ENSP00000340554.6:p.Cys22732Ter
|
|
ENST00000342992.10:c.87111C>A
(TTN)
|
ENSP00000343764.6:p.Cys29037Ter
|
|
ENST00000359218.9:c.67995C>A
(TTN)
|
ENSP00000352154.5:p.Cys22665Ter
|
|
ENST00000460472.6:c.67620C>A
(TTN)
|
ENSP00000434586.1:p.Cys22540Ter
|
|
ENST00000589042.5:c.94815C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Cys31605Ter
|
|
ENST00000591111.5:c.89892C>A
(TTN)
|
ENSP00000465570.1:p.Cys29964Ter
|
|
ENST00000615779.4:c.89892C>A
(TTN)
|
ENSP00000483597.1:p.Cys29964Ter
|
|
NM_001256850.1:c.89892C>A
(TTN)
|
NP_001243779.1:p.Cys29964Ter
|
|
NM_001267550.2:c.94815C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Cys31605Ter
|
|
NM_003319.4:c.67620C>A
(TTN)
|
NP_003310.4:p.Cys22540Ter
|
|
NM_133378.4:c.87111C>A
(TTN)
|
NP_596869.4:p.Cys29037Ter
|
|
NM_133432.3:c.67995C>A
(TTN)
|
NP_597676.3:p.Cys22665Ter
|
|
NM_133437.4:c.68196C>A
(TTN)
|
NP_597681.4:p.Cys22732Ter
|
|
NR_038271.1:n.446+22977G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4252G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.93912C>A
(TTN)
|
XP_011510031.1:p.Cys31304Ter
|
|
XM_011511730.1:c.67806C>A
(TTN)
|
XP_011510032.1:p.Cys22602Ter
|
|
XM_011511731.1:c.67665C>A
(TTN)
|
XP_011510033.1:p.Cys22555Ter
|
|
XM_017004819.1:c.93708C>A
(TTN)
|
XP_016860308.1:p.Cys31236Ter
|
|
XM_017004820.1:c.89106C>A
(TTN)
|
XP_016860309.1:p.Cys29702Ter
|
|
XM_017004821.1:c.89103C>A
(TTN)
|
XP_016860310.1:p.Cys29701Ter
|
|
XM_017004822.1:c.86145C>A
(TTN)
|
XP_016860311.1:p.Cys28715Ter
|
|
XM_017004823.1:c.67761C>A
(TTN)
|
XP_016860312.1:p.Cys22587Ter
|
|
XM_024453094.1:c.89256C>A
(TTN)
|
XP_024308862.1:p.Cys29752Ter
|
|
XM_024453095.1:c.89253C>A
(TTN)
|
XP_024308863.1:p.Cys29751Ter
|
|
XM_024453096.1:c.88686C>A
(TTN)
|
XP_024308864.1:p.Cys29562Ter
|
|
XM_024453097.1:c.86028C>A
(TTN)
|
XP_024308865.1:p.Cys28676Ter
|
|
XM_024453098.1:c.85947C>A
(TTN)
|
XP_024308866.1:p.Cys28649Ter
|
|
XM_024453099.1:c.67710C>A
(TTN)
|
XP_024308867.1:p.Cys22570Ter
|
|
XM_024453100.1:c.57564C>A
(TTN)
|
XP_024308868.1:p.Cys19188Ter
|
|