ENST00000342992.11:c.84188A>G
(TTN)
|
ENSP00000343764.6:p.Asn28063Ser
|
|
ENST00000342175.11:c.65273A>G
(TTN)
|
ENSP00000340554.6:p.Asn21758Ser
|
|
ENST00000359218.10:c.65072A>G
(TTN)
|
ENSP00000352154.5:p.Asn21691Ser
|
|
ENST00000342175.10:c.65273A>G
(TTN)
|
ENSP00000340554.6:p.Asn21758Ser
|
|
ENST00000342992.10:c.84188A>G
(TTN)
|
ENSP00000343764.6:p.Asn28063Ser
|
|
ENST00000359218.9:c.65072A>G
(TTN)
|
ENSP00000352154.5:p.Asn21691Ser
|
|
ENST00000460472.6:c.64697A>G
(TTN)
|
ENSP00000434586.1:p.Asn21566Ser
|
|
ENST00000589042.5:c.91892A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn30631Ser
|
|
ENST00000591111.5:c.86969A>G
(TTN)
|
ENSP00000465570.1:p.Asn28990Ser
|
|
ENST00000615779.4:c.86969A>G
(TTN)
|
ENSP00000483597.1:p.Asn28990Ser
|
|
NM_001256850.1:c.86969A>G
(TTN)
|
NP_001243779.1:p.Asn28990Ser
|
|
NM_001267550.2:c.91892A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asn30631Ser
|
|
NM_003319.4:c.64697A>G
(TTN)
|
NP_003310.4:p.Asn21566Ser
|
|
NM_133378.4:c.84188A>G
(TTN)
|
NP_596869.4:p.Asn28063Ser
|
|
NM_133432.3:c.65072A>G
(TTN)
|
NP_597676.3:p.Asn21691Ser
|
|
NM_133437.4:c.65273A>G
(TTN)
|
NP_597681.4:p.Asn21758Ser
|
|
NR_038271.1:n.447-21470T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+7469T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90989A>G
(TTN)
|
XP_011510031.1:p.Asn30330Ser
|
|
XM_011511730.1:c.64883A>G
(TTN)
|
XP_011510032.1:p.Asn21628Ser
|
|
XM_011511731.1:c.64742A>G
(TTN)
|
XP_011510033.1:p.Asn21581Ser
|
|
XM_017004819.1:c.90785A>G
(TTN)
|
XP_016860308.1:p.Asn30262Ser
|
|
XM_017004820.1:c.86183A>G
(TTN)
|
XP_016860309.1:p.Asn28728Ser
|
|
XM_017004821.1:c.86180A>G
(TTN)
|
XP_016860310.1:p.Asn28727Ser
|
|
XM_017004822.1:c.83222A>G
(TTN)
|
XP_016860311.1:p.Asn27741Ser
|
|
XM_017004823.1:c.64838A>G
(TTN)
|
XP_016860312.1:p.Asn21613Ser
|
|
XM_024453094.1:c.86333A>G
(TTN)
|
XP_024308862.1:p.Asn28778Ser
|
|
XM_024453095.1:c.86330A>G
(TTN)
|
XP_024308863.1:p.Asn28777Ser
|
|
XM_024453096.1:c.85763A>G
(TTN)
|
XP_024308864.1:p.Asn28588Ser
|
|
XM_024453097.1:c.83105A>G
(TTN)
|
XP_024308865.1:p.Asn27702Ser
|
|
XM_024453098.1:c.83024A>G
(TTN)
|
XP_024308866.1:p.Asn27675Ser
|
|
XM_024453099.1:c.64787A>G
(TTN)
|
XP_024308867.1:p.Asn21596Ser
|
|
XM_024453100.1:c.54641A>G
(TTN)
|
XP_024308868.1:p.Asn18214Ser
|
|