ENST00000342992.11:c.93117T>A
(TTN)
|
ENSP00000343764.6:p.Ala31039=
|
|
ENST00000342175.11:c.74202T>A
(TTN)
|
ENSP00000340554.6:p.Ala24734=
|
|
ENST00000359218.10:c.74001T>A
(TTN)
|
ENSP00000352154.5:p.Ala24667=
|
|
ENST00000342175.10:c.74202T>A
(TTN)
|
ENSP00000340554.6:p.Ala24734=
|
|
ENST00000342992.10:c.93117T>A
(TTN)
|
ENSP00000343764.6:p.Ala31039=
|
|
ENST00000359218.9:c.74001T>A
(TTN)
|
ENSP00000352154.5:p.Ala24667=
|
|
ENST00000460472.6:c.73626T>A
(TTN)
|
ENSP00000434586.1:p.Ala24542=
|
|
ENST00000589042.5:c.100821T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala33607=
|
|
ENST00000591111.5:c.95898T>A
(TTN)
|
ENSP00000465570.1:p.Ala31966=
|
|
ENST00000615779.4:c.95898T>A
(TTN)
|
ENSP00000483597.1:p.Ala31966=
|
|
NM_001256850.1:c.95898T>A
(TTN)
|
NP_001243779.1:p.Ala31966=
|
|
NM_001267550.2:c.100821T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala33607=
|
|
NM_003319.4:c.73626T>A
(TTN)
|
NP_003310.4:p.Ala24542=
|
|
NM_133378.4:c.93117T>A
(TTN)
|
NP_596869.4:p.Ala31039=
|
|
NM_133432.3:c.74001T>A
(TTN)
|
NP_597676.3:p.Ala24667=
|
|
NM_133437.4:c.74202T>A
(TTN)
|
NP_597681.4:p.Ala24734=
|
|
NR_038271.1:n.446+12158A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.282A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.99918T>A
(TTN)
|
XP_011510031.1:p.Ala33306=
|
|
XM_011511730.1:c.73812T>A
(TTN)
|
XP_011510032.1:p.Ala24604=
|
|
XM_011511731.1:c.73671T>A
(TTN)
|
XP_011510033.1:p.Ala24557=
|
|
XM_017004819.1:c.99714T>A
(TTN)
|
XP_016860308.1:p.Ala33238=
|
|
XM_017004820.1:c.95112T>A
(TTN)
|
XP_016860309.1:p.Ala31704=
|
|
XM_017004821.1:c.95109T>A
(TTN)
|
XP_016860310.1:p.Ala31703=
|
|
XM_017004822.1:c.92151T>A
(TTN)
|
XP_016860311.1:p.Ala30717=
|
|
XM_017004823.1:c.73767T>A
(TTN)
|
XP_016860312.1:p.Ala24589=
|
|
XM_024453094.1:c.95262T>A
(TTN)
|
XP_024308862.1:p.Ala31754=
|
|
XM_024453095.1:c.95259T>A
(TTN)
|
XP_024308863.1:p.Ala31753=
|
|
XM_024453096.1:c.94692T>A
(TTN)
|
XP_024308864.1:p.Ala31564=
|
|
XM_024453097.1:c.92034T>A
(TTN)
|
XP_024308865.1:p.Ala30678=
|
|
XM_024453098.1:c.91953T>A
(TTN)
|
XP_024308866.1:p.Ala30651=
|
|
XM_024453099.1:c.73716T>A
(TTN)
|
XP_024308867.1:p.Ala24572=
|
|
XM_024453100.1:c.63570T>A
(TTN)
|
XP_024308868.1:p.Ala21190=
|
|