ENST00000342992.11:c.88256C>A
(TTN)
|
ENSP00000343764.6:p.Ala29419Asp
|
|
ENST00000342175.11:c.69341C>A
(TTN)
|
ENSP00000340554.6:p.Ala23114Asp
|
|
ENST00000359218.10:c.69140C>A
(TTN)
|
ENSP00000352154.5:p.Ala23047Asp
|
|
ENST00000342175.10:c.69341C>A
(TTN)
|
ENSP00000340554.6:p.Ala23114Asp
|
|
ENST00000342992.10:c.88256C>A
(TTN)
|
ENSP00000343764.6:p.Ala29419Asp
|
|
ENST00000359218.9:c.69140C>A
(TTN)
|
ENSP00000352154.5:p.Ala23047Asp
|
|
ENST00000460472.6:c.68765C>A
(TTN)
|
ENSP00000434586.1:p.Ala22922Asp
|
|
ENST00000589042.5:c.95960C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala31987Asp
|
|
ENST00000591111.5:c.91037C>A
(TTN)
|
ENSP00000465570.1:p.Ala30346Asp
|
|
ENST00000615779.4:c.91037C>A
(TTN)
|
ENSP00000483597.1:p.Ala30346Asp
|
|
NM_001256850.1:c.91037C>A
(TTN)
|
NP_001243779.1:p.Ala30346Asp
|
|
NM_001267550.2:c.95960C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala31987Asp
|
|
NM_003319.4:c.68765C>A
(TTN)
|
NP_003310.4:p.Ala22922Asp
|
|
NM_133378.4:c.88256C>A
(TTN)
|
NP_596869.4:p.Ala29419Asp
|
|
NM_133432.3:c.69140C>A
(TTN)
|
NP_597676.3:p.Ala23047Asp
|
|
NM_133437.4:c.69341C>A
(TTN)
|
NP_597681.4:p.Ala23114Asp
|
|
NR_038271.1:n.446+20633G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1908G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.95057C>A
(TTN)
|
XP_011510031.1:p.Ala31686Asp
|
|
XM_011511730.1:c.68951C>A
(TTN)
|
XP_011510032.1:p.Ala22984Asp
|
|
XM_011511731.1:c.68810C>A
(TTN)
|
XP_011510033.1:p.Ala22937Asp
|
|
XM_017004819.1:c.94853C>A
(TTN)
|
XP_016860308.1:p.Ala31618Asp
|
|
XM_017004820.1:c.90251C>A
(TTN)
|
XP_016860309.1:p.Ala30084Asp
|
|
XM_017004821.1:c.90248C>A
(TTN)
|
XP_016860310.1:p.Ala30083Asp
|
|
XM_017004822.1:c.87290C>A
(TTN)
|
XP_016860311.1:p.Ala29097Asp
|
|
XM_017004823.1:c.68906C>A
(TTN)
|
XP_016860312.1:p.Ala22969Asp
|
|
XM_024453094.1:c.90401C>A
(TTN)
|
XP_024308862.1:p.Ala30134Asp
|
|
XM_024453095.1:c.90398C>A
(TTN)
|
XP_024308863.1:p.Ala30133Asp
|
|
XM_024453096.1:c.89831C>A
(TTN)
|
XP_024308864.1:p.Ala29944Asp
|
|
XM_024453097.1:c.87173C>A
(TTN)
|
XP_024308865.1:p.Ala29058Asp
|
|
XM_024453098.1:c.87092C>A
(TTN)
|
XP_024308866.1:p.Ala29031Asp
|
|
XM_024453099.1:c.68855C>A
(TTN)
|
XP_024308867.1:p.Ala22952Asp
|
|
XM_024453100.1:c.58709C>A
(TTN)
|
XP_024308868.1:p.Ala19570Asp
|
|