ENST00000342992.11:c.88184C>G
(TTN)
|
ENSP00000343764.6:p.Ala29395Gly
|
|
ENST00000342175.11:c.69269C>G
(TTN)
|
ENSP00000340554.6:p.Ala23090Gly
|
|
ENST00000359218.10:c.69068C>G
(TTN)
|
ENSP00000352154.5:p.Ala23023Gly
|
|
ENST00000342175.10:c.69269C>G
(TTN)
|
ENSP00000340554.6:p.Ala23090Gly
|
|
ENST00000342992.10:c.88184C>G
(TTN)
|
ENSP00000343764.6:p.Ala29395Gly
|
|
ENST00000359218.9:c.69068C>G
(TTN)
|
ENSP00000352154.5:p.Ala23023Gly
|
|
ENST00000460472.6:c.68693C>G
(TTN)
|
ENSP00000434586.1:p.Ala22898Gly
|
|
ENST00000589042.5:c.95888C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala31963Gly
|
|
ENST00000591111.5:c.90965C>G
(TTN)
|
ENSP00000465570.1:p.Ala30322Gly
|
|
ENST00000615779.4:c.90965C>G
(TTN)
|
ENSP00000483597.1:p.Ala30322Gly
|
|
NM_001256850.1:c.90965C>G
(TTN)
|
NP_001243779.1:p.Ala30322Gly
|
|
NM_001267550.2:c.95888C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ala31963Gly
|
|
NM_003319.4:c.68693C>G
(TTN)
|
NP_003310.4:p.Ala22898Gly
|
|
NM_133378.4:c.88184C>G
(TTN)
|
NP_596869.4:p.Ala29395Gly
|
|
NM_133432.3:c.69068C>G
(TTN)
|
NP_597676.3:p.Ala23023Gly
|
|
NM_133437.4:c.69269C>G
(TTN)
|
NP_597681.4:p.Ala23090Gly
|
|
NR_038271.1:n.446+20705G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1980G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.94985C>G
(TTN)
|
XP_011510031.1:p.Ala31662Gly
|
|
XM_011511730.1:c.68879C>G
(TTN)
|
XP_011510032.1:p.Ala22960Gly
|
|
XM_011511731.1:c.68738C>G
(TTN)
|
XP_011510033.1:p.Ala22913Gly
|
|
XM_017004819.1:c.94781C>G
(TTN)
|
XP_016860308.1:p.Ala31594Gly
|
|
XM_017004820.1:c.90179C>G
(TTN)
|
XP_016860309.1:p.Ala30060Gly
|
|
XM_017004821.1:c.90176C>G
(TTN)
|
XP_016860310.1:p.Ala30059Gly
|
|
XM_017004822.1:c.87218C>G
(TTN)
|
XP_016860311.1:p.Ala29073Gly
|
|
XM_017004823.1:c.68834C>G
(TTN)
|
XP_016860312.1:p.Ala22945Gly
|
|
XM_024453094.1:c.90329C>G
(TTN)
|
XP_024308862.1:p.Ala30110Gly
|
|
XM_024453095.1:c.90326C>G
(TTN)
|
XP_024308863.1:p.Ala30109Gly
|
|
XM_024453096.1:c.89759C>G
(TTN)
|
XP_024308864.1:p.Ala29920Gly
|
|
XM_024453097.1:c.87101C>G
(TTN)
|
XP_024308865.1:p.Ala29034Gly
|
|
XM_024453098.1:c.87020C>G
(TTN)
|
XP_024308866.1:p.Ala29007Gly
|
|
XM_024453099.1:c.68783C>G
(TTN)
|
XP_024308867.1:p.Ala22928Gly
|
|
XM_024453100.1:c.58637C>G
(TTN)
|
XP_024308868.1:p.Ala19546Gly
|
|