ENST00000342992.11:c.64457C>A
(TTN)
|
ENSP00000343764.6:p.Ser21486Ter
|
|
ENST00000342175.11:c.45542C>A
(TTN)
|
ENSP00000340554.6:p.Ser15181Ter
|
|
ENST00000359218.10:c.45341C>A
(TTN)
|
ENSP00000352154.5:p.Ser15114Ter
|
|
ENST00000342175.10:c.45542C>A
(TTN)
|
ENSP00000340554.6:p.Ser15181Ter
|
|
ENST00000342992.10:c.64457C>A
(TTN)
|
ENSP00000343764.6:p.Ser21486Ter
|
|
ENST00000359218.9:c.45341C>A
(TTN)
|
ENSP00000352154.5:p.Ser15114Ter
|
|
ENST00000460472.6:c.44966C>A
(TTN)
|
ENSP00000434586.1:p.Ser14989Ter
|
|
ENST00000589042.5:c.72161C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser24054Ter
|
|
ENST00000591111.5:c.67238C>A
(TTN)
|
ENSP00000465570.1:p.Ser22413Ter
|
|
ENST00000615779.4:c.67238C>A
(TTN)
|
ENSP00000483597.1:p.Ser22413Ter
|
|
NM_001256850.1:c.67238C>A
(TTN)
|
NP_001243779.1:p.Ser22413Ter
|
|
NM_001267550.2:c.72161C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser24054Ter
|
|
NM_003319.4:c.44966C>A
(TTN)
|
NP_003310.4:p.Ser14989Ter
|
|
NM_133378.4:c.64457C>A
(TTN)
|
NP_596869.4:p.Ser21486Ter
|
|
NM_133432.3:c.45341C>A
(TTN)
|
NP_597676.3:p.Ser15114Ter
|
|
NM_133437.4:c.45542C>A
(TTN)
|
NP_597681.4:p.Ser15181Ter
|
|
NR_038271.1:n.596+2522G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-8601G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.71258C>A
(TTN)
|
XP_011510031.1:p.Ser23753Ter
|
|
XM_011511730.1:c.45152C>A
(TTN)
|
XP_011510032.1:p.Ser15051Ter
|
|
XM_011511731.1:c.45011C>A
(TTN)
|
XP_011510033.1:p.Ser15004Ter
|
|
XM_017004819.1:c.71054C>A
(TTN)
|
XP_016860308.1:p.Ser23685Ter
|
|
XM_017004820.1:c.66452C>A
(TTN)
|
XP_016860309.1:p.Ser22151Ter
|
|
XM_017004821.1:c.66449C>A
(TTN)
|
XP_016860310.1:p.Ser22150Ter
|
|
XM_017004822.1:c.63491C>A
(TTN)
|
XP_016860311.1:p.Ser21164Ter
|
|
XM_017004823.1:c.45107C>A
(TTN)
|
XP_016860312.1:p.Ser15036Ter
|
|
XM_024453094.1:c.66602C>A
(TTN)
|
XP_024308862.1:p.Ser22201Ter
|
|
XM_024453095.1:c.66599C>A
(TTN)
|
XP_024308863.1:p.Ser22200Ter
|
|
XM_024453096.1:c.66032C>A
(TTN)
|
XP_024308864.1:p.Ser22011Ter
|
|
XM_024453097.1:c.63374C>A
(TTN)
|
XP_024308865.1:p.Ser21125Ter
|
|
XM_024453098.1:c.63293C>A
(TTN)
|
XP_024308866.1:p.Ser21098Ter
|
|
XM_024453099.1:c.45056C>A
(TTN)
|
XP_024308867.1:p.Ser15019Ter
|
|
XM_024453100.1:c.34910C>A
(TTN)
|
XP_024308868.1:p.Ser11637Ter
|
|