ENST00000342992.11:c.88605T>G
(TTN)
|
ENSP00000343764.6:p.Tyr29535Ter
|
|
ENST00000342175.11:c.69690T>G
(TTN)
|
ENSP00000340554.6:p.Tyr23230Ter
|
|
ENST00000359218.10:c.69489T>G
(TTN)
|
ENSP00000352154.5:p.Tyr23163Ter
|
|
ENST00000342175.10:c.69690T>G
(TTN)
|
ENSP00000340554.6:p.Tyr23230Ter
|
|
ENST00000342992.10:c.88605T>G
(TTN)
|
ENSP00000343764.6:p.Tyr29535Ter
|
|
ENST00000359218.9:c.69489T>G
(TTN)
|
ENSP00000352154.5:p.Tyr23163Ter
|
|
ENST00000460472.6:c.69114T>G
(TTN)
|
ENSP00000434586.1:p.Tyr23038Ter
|
|
ENST00000589042.5:c.96309T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr32103Ter
|
|
ENST00000591111.5:c.91386T>G
(TTN)
|
ENSP00000465570.1:p.Tyr30462Ter
|
|
ENST00000615779.4:c.91386T>G
(TTN)
|
ENSP00000483597.1:p.Tyr30462Ter
|
|
NM_001256850.1:c.91386T>G
(TTN)
|
NP_001243779.1:p.Tyr30462Ter
|
|
NM_001267550.2:c.96309T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr32103Ter
|
|
NM_003319.4:c.69114T>G
(TTN)
|
NP_003310.4:p.Tyr23038Ter
|
|
NM_133378.4:c.88605T>G
(TTN)
|
NP_596869.4:p.Tyr29535Ter
|
|
NM_133432.3:c.69489T>G
(TTN)
|
NP_597676.3:p.Tyr23163Ter
|
|
NM_133437.4:c.69690T>G
(TTN)
|
NP_597681.4:p.Tyr23230Ter
|
|
NR_038271.1:n.446+20199A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1474A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95406T>G
(TTN)
|
XP_011510031.1:p.Tyr31802Ter
|
|
XM_011511730.1:c.69300T>G
(TTN)
|
XP_011510032.1:p.Tyr23100Ter
|
|
XM_011511731.1:c.69159T>G
(TTN)
|
XP_011510033.1:p.Tyr23053Ter
|
|
XM_017004819.1:c.95202T>G
(TTN)
|
XP_016860308.1:p.Tyr31734Ter
|
|
XM_017004820.1:c.90600T>G
(TTN)
|
XP_016860309.1:p.Tyr30200Ter
|
|
XM_017004821.1:c.90597T>G
(TTN)
|
XP_016860310.1:p.Tyr30199Ter
|
|
XM_017004822.1:c.87639T>G
(TTN)
|
XP_016860311.1:p.Tyr29213Ter
|
|
XM_017004823.1:c.69255T>G
(TTN)
|
XP_016860312.1:p.Tyr23085Ter
|
|
XM_024453094.1:c.90750T>G
(TTN)
|
XP_024308862.1:p.Tyr30250Ter
|
|
XM_024453095.1:c.90747T>G
(TTN)
|
XP_024308863.1:p.Tyr30249Ter
|
|
XM_024453096.1:c.90180T>G
(TTN)
|
XP_024308864.1:p.Tyr30060Ter
|
|
XM_024453097.1:c.87522T>G
(TTN)
|
XP_024308865.1:p.Tyr29174Ter
|
|
XM_024453098.1:c.87441T>G
(TTN)
|
XP_024308866.1:p.Tyr29147Ter
|
|
XM_024453099.1:c.69204T>G
(TTN)
|
XP_024308867.1:p.Tyr23068Ter
|
|
XM_024453100.1:c.59058T>G
(TTN)
|
XP_024308868.1:p.Tyr19686Ter
|
|