ENST00000342992.11:c.51341G>A
(TTN)
|
ENSP00000343764.6:p.Ser17114Asn
|
|
ENST00000342175.11:c.32426G>A
(TTN)
|
ENSP00000340554.6:p.Ser10809Asn
|
|
ENST00000359218.10:c.32225G>A
(TTN)
|
ENSP00000352154.5:p.Ser10742Asn
|
|
ENST00000342175.10:c.32426G>A
(TTN)
|
ENSP00000340554.6:p.Ser10809Asn
|
|
ENST00000342992.10:c.51341G>A
(TTN)
|
ENSP00000343764.6:p.Ser17114Asn
|
|
ENST00000359218.9:c.32225G>A
(TTN)
|
ENSP00000352154.5:p.Ser10742Asn
|
|
ENST00000460472.6:c.31850G>A
(TTN)
|
ENSP00000434586.1:p.Ser10617Asn
|
|
ENST00000589042.5:c.59045G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser19682Asn
|
|
ENST00000591111.5:c.54122G>A
(TTN)
|
ENSP00000465570.1:p.Ser18041Asn
|
|
ENST00000615779.4:c.54122G>A
(TTN)
|
ENSP00000483597.1:p.Ser18041Asn
|
|
NM_001256850.1:c.54122G>A
(TTN)
|
NP_001243779.1:p.Ser18041Asn
|
|
NM_001267550.2:c.59045G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser19682Asn
|
|
NM_003319.4:c.31850G>A
(TTN)
|
NP_003310.4:p.Ser10617Asn
|
|
NM_133378.4:c.51341G>A
(TTN)
|
NP_596869.4:p.Ser17114Asn
|
|
NM_133432.3:c.32225G>A
(TTN)
|
NP_597676.3:p.Ser10742Asn
|
|
NM_133437.4:c.32426G>A
(TTN)
|
NP_597681.4:p.Ser10809Asn
|
|
NR_038271.1:n.597-4522C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1760C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58142G>A
(TTN)
|
XP_011510031.1:p.Ser19381Asn
|
|
XM_011511730.1:c.32036G>A
(TTN)
|
XP_011510032.1:p.Ser10679Asn
|
|
XM_011511731.1:c.31895G>A
(TTN)
|
XP_011510033.1:p.Ser10632Asn
|
|
XM_017004819.1:c.57938G>A
(TTN)
|
XP_016860308.1:p.Ser19313Asn
|
|
XM_017004820.1:c.53336G>A
(TTN)
|
XP_016860309.1:p.Ser17779Asn
|
|
XM_017004821.1:c.53333G>A
(TTN)
|
XP_016860310.1:p.Ser17778Asn
|
|
XM_017004822.1:c.50375G>A
(TTN)
|
XP_016860311.1:p.Ser16792Asn
|
|
XM_017004823.1:c.31991G>A
(TTN)
|
XP_016860312.1:p.Ser10664Asn
|
|
XM_024453094.1:c.53486G>A
(TTN)
|
XP_024308862.1:p.Ser17829Asn
|
|
XM_024453095.1:c.53483G>A
(TTN)
|
XP_024308863.1:p.Ser17828Asn
|
|
XM_024453096.1:c.52916G>A
(TTN)
|
XP_024308864.1:p.Ser17639Asn
|
|
XM_024453097.1:c.50258G>A
(TTN)
|
XP_024308865.1:p.Ser16753Asn
|
|
XM_024453098.1:c.50177G>A
(TTN)
|
XP_024308866.1:p.Ser16726Asn
|
|
XM_024453099.1:c.31940G>A
(TTN)
|
XP_024308867.1:p.Ser10647Asn
|
|
XM_024453100.1:c.21794G>A
(TTN)
|
XP_024308868.1:p.Ser7265Asn
|
|