ENST00000342992.11:c.98388A>T
(TTN)
|
ENSP00000343764.6:p.Glu32796Asp
|
|
ENST00000342175.11:c.79473A>T
(TTN)
|
ENSP00000340554.6:p.Glu26491Asp
|
|
ENST00000359218.10:c.79272A>T
(TTN)
|
ENSP00000352154.5:p.Glu26424Asp
|
|
ENST00000342175.10:c.79473A>T
(TTN)
|
ENSP00000340554.6:p.Glu26491Asp
|
|
ENST00000342992.10:c.98388A>T
(TTN)
|
ENSP00000343764.6:p.Glu32796Asp
|
|
ENST00000359218.9:c.79272A>T
(TTN)
|
ENSP00000352154.5:p.Glu26424Asp
|
|
ENST00000460472.6:c.78897A>T
(TTN)
|
ENSP00000434586.1:p.Glu26299Asp
|
|
ENST00000589042.5:c.106092A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu35364Asp
|
|
ENST00000591111.5:c.101169A>T
(TTN)
|
ENSP00000465570.1:p.Glu33723Asp
|
|
ENST00000615779.4:c.101169A>T
(TTN)
|
ENSP00000483597.1:p.Glu33723Asp
|
|
NM_001256850.1:c.101169A>T
(TTN)
|
NP_001243779.1:p.Glu33723Asp
|
|
NM_001267550.2:c.106092A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu35364Asp
|
|
NM_003319.4:c.78897A>T
(TTN)
|
NP_003310.4:p.Glu26299Asp
|
|
NM_133378.4:c.98388A>T
(TTN)
|
NP_596869.4:p.Glu32796Asp
|
|
NM_133432.3:c.79272A>T
(TTN)
|
NP_597676.3:p.Glu26424Asp
|
|
NM_133437.4:c.79473A>T
(TTN)
|
NP_597681.4:p.Glu26491Asp
|
|
NR_038271.1:n.446+6887T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5209T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105189A>T
(TTN)
|
XP_011510031.1:p.Glu35063Asp
|
|
XM_011511730.1:c.79083A>T
(TTN)
|
XP_011510032.1:p.Glu26361Asp
|
|
XM_011511731.1:c.78942A>T
(TTN)
|
XP_011510033.1:p.Glu26314Asp
|
|
XM_017004819.1:c.104985A>T
(TTN)
|
XP_016860308.1:p.Glu34995Asp
|
|
XM_017004820.1:c.100383A>T
(TTN)
|
XP_016860309.1:p.Glu33461Asp
|
|
XM_017004821.1:c.100380A>T
(TTN)
|
XP_016860310.1:p.Glu33460Asp
|
|
XM_017004822.1:c.97422A>T
(TTN)
|
XP_016860311.1:p.Glu32474Asp
|
|
XM_017004823.1:c.79038A>T
(TTN)
|
XP_016860312.1:p.Glu26346Asp
|
|
XM_024453094.1:c.100533A>T
(TTN)
|
XP_024308862.1:p.Glu33511Asp
|
|
XM_024453095.1:c.100530A>T
(TTN)
|
XP_024308863.1:p.Glu33510Asp
|
|
XM_024453096.1:c.99963A>T
(TTN)
|
XP_024308864.1:p.Glu33321Asp
|
|
XM_024453097.1:c.97305A>T
(TTN)
|
XP_024308865.1:p.Glu32435Asp
|
|
XM_024453098.1:c.97224A>T
(TTN)
|
XP_024308866.1:p.Glu32408Asp
|
|
XM_024453099.1:c.78987A>T
(TTN)
|
XP_024308867.1:p.Glu26329Asp
|
|
XM_024453100.1:c.68841A>T
(TTN)
|
XP_024308868.1:p.Glu22947Asp
|
|