ENST00000342992.11:c.98665G>T
(TTN)
|
ENSP00000343764.6:p.Gly32889Ter
|
|
ENST00000342175.11:c.79750G>T
(TTN)
|
ENSP00000340554.6:p.Gly26584Ter
|
|
ENST00000359218.10:c.79549G>T
(TTN)
|
ENSP00000352154.5:p.Gly26517Ter
|
|
ENST00000342175.10:c.79750G>T
(TTN)
|
ENSP00000340554.6:p.Gly26584Ter
|
|
ENST00000342992.10:c.98665G>T
(TTN)
|
ENSP00000343764.6:p.Gly32889Ter
|
|
ENST00000359218.9:c.79549G>T
(TTN)
|
ENSP00000352154.5:p.Gly26517Ter
|
|
ENST00000460472.6:c.79174G>T
(TTN)
|
ENSP00000434586.1:p.Gly26392Ter
|
|
ENST00000589042.5:c.106369G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly35457Ter
|
|
ENST00000591111.5:c.101446G>T
(TTN)
|
ENSP00000465570.1:p.Gly33816Ter
|
|
ENST00000615779.4:c.101446G>T
(TTN)
|
ENSP00000483597.1:p.Gly33816Ter
|
|
NM_001256850.1:c.101446G>T
(TTN)
|
NP_001243779.1:p.Gly33816Ter
|
|
NM_001267550.2:c.106369G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Gly35457Ter
|
|
NM_003319.4:c.79174G>T
(TTN)
|
NP_003310.4:p.Gly26392Ter
|
|
NM_133378.4:c.98665G>T
(TTN)
|
NP_596869.4:p.Gly32889Ter
|
|
NM_133432.3:c.79549G>T
(TTN)
|
NP_597676.3:p.Gly26517Ter
|
|
NM_133437.4:c.79750G>T
(TTN)
|
NP_597681.4:p.Gly26584Ter
|
|
NR_038271.1:n.446+6610C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5486C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105466G>T
(TTN)
|
XP_011510031.1:p.Gly35156Ter
|
|
XM_011511730.1:c.79360G>T
(TTN)
|
XP_011510032.1:p.Gly26454Ter
|
|
XM_011511731.1:c.79219G>T
(TTN)
|
XP_011510033.1:p.Gly26407Ter
|
|
XM_017004819.1:c.105262G>T
(TTN)
|
XP_016860308.1:p.Gly35088Ter
|
|
XM_017004820.1:c.100660G>T
(TTN)
|
XP_016860309.1:p.Gly33554Ter
|
|
XM_017004821.1:c.100657G>T
(TTN)
|
XP_016860310.1:p.Gly33553Ter
|
|
XM_017004822.1:c.97699G>T
(TTN)
|
XP_016860311.1:p.Gly32567Ter
|
|
XM_017004823.1:c.79315G>T
(TTN)
|
XP_016860312.1:p.Gly26439Ter
|
|
XM_024453094.1:c.100810G>T
(TTN)
|
XP_024308862.1:p.Gly33604Ter
|
|
XM_024453095.1:c.100807G>T
(TTN)
|
XP_024308863.1:p.Gly33603Ter
|
|
XM_024453096.1:c.100240G>T
(TTN)
|
XP_024308864.1:p.Gly33414Ter
|
|
XM_024453097.1:c.97582G>T
(TTN)
|
XP_024308865.1:p.Gly32528Ter
|
|
XM_024453098.1:c.97501G>T
(TTN)
|
XP_024308866.1:p.Gly32501Ter
|
|
XM_024453099.1:c.79264G>T
(TTN)
|
XP_024308867.1:p.Gly26422Ter
|
|
XM_024453100.1:c.69118G>T
(TTN)
|
XP_024308868.1:p.Gly23040Ter
|
|