ENST00000342992.11:c.88208C>A
(TTN)
|
ENSP00000343764.6:p.Thr29403Asn
|
|
ENST00000342175.11:c.69293C>A
(TTN)
|
ENSP00000340554.6:p.Thr23098Asn
|
|
ENST00000359218.10:c.69092C>A
(TTN)
|
ENSP00000352154.5:p.Thr23031Asn
|
|
ENST00000342175.10:c.69293C>A
(TTN)
|
ENSP00000340554.6:p.Thr23098Asn
|
|
ENST00000342992.10:c.88208C>A
(TTN)
|
ENSP00000343764.6:p.Thr29403Asn
|
|
ENST00000359218.9:c.69092C>A
(TTN)
|
ENSP00000352154.5:p.Thr23031Asn
|
|
ENST00000460472.6:c.68717C>A
(TTN)
|
ENSP00000434586.1:p.Thr22906Asn
|
|
ENST00000589042.5:c.95912C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31971Asn
|
|
ENST00000591111.5:c.90989C>A
(TTN)
|
ENSP00000465570.1:p.Thr30330Asn
|
|
ENST00000615779.4:c.90989C>A
(TTN)
|
ENSP00000483597.1:p.Thr30330Asn
|
|
NM_001256850.1:c.90989C>A
(TTN)
|
NP_001243779.1:p.Thr30330Asn
|
|
NM_001267550.2:c.95912C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31971Asn
|
|
NM_003319.4:c.68717C>A
(TTN)
|
NP_003310.4:p.Thr22906Asn
|
|
NM_133378.4:c.88208C>A
(TTN)
|
NP_596869.4:p.Thr29403Asn
|
|
NM_133432.3:c.69092C>A
(TTN)
|
NP_597676.3:p.Thr23031Asn
|
|
NM_133437.4:c.69293C>A
(TTN)
|
NP_597681.4:p.Thr23098Asn
|
|
NR_038271.1:n.446+20681G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1956G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.95009C>A
(TTN)
|
XP_011510031.1:p.Thr31670Asn
|
|
XM_011511730.1:c.68903C>A
(TTN)
|
XP_011510032.1:p.Thr22968Asn
|
|
XM_011511731.1:c.68762C>A
(TTN)
|
XP_011510033.1:p.Thr22921Asn
|
|
XM_017004819.1:c.94805C>A
(TTN)
|
XP_016860308.1:p.Thr31602Asn
|
|
XM_017004820.1:c.90203C>A
(TTN)
|
XP_016860309.1:p.Thr30068Asn
|
|
XM_017004821.1:c.90200C>A
(TTN)
|
XP_016860310.1:p.Thr30067Asn
|
|
XM_017004822.1:c.87242C>A
(TTN)
|
XP_016860311.1:p.Thr29081Asn
|
|
XM_017004823.1:c.68858C>A
(TTN)
|
XP_016860312.1:p.Thr22953Asn
|
|
XM_024453094.1:c.90353C>A
(TTN)
|
XP_024308862.1:p.Thr30118Asn
|
|
XM_024453095.1:c.90350C>A
(TTN)
|
XP_024308863.1:p.Thr30117Asn
|
|
XM_024453096.1:c.89783C>A
(TTN)
|
XP_024308864.1:p.Thr29928Asn
|
|
XM_024453097.1:c.87125C>A
(TTN)
|
XP_024308865.1:p.Thr29042Asn
|
|
XM_024453098.1:c.87044C>A
(TTN)
|
XP_024308866.1:p.Thr29015Asn
|
|
XM_024453099.1:c.68807C>A
(TTN)
|
XP_024308867.1:p.Thr22936Asn
|
|
XM_024453100.1:c.58661C>A
(TTN)
|
XP_024308868.1:p.Thr19554Asn
|
|