ENST00000342992.11:c.88326A>T
(TTN)
|
ENSP00000343764.6:p.Glu29442Asp
|
|
ENST00000342175.11:c.69411A>T
(TTN)
|
ENSP00000340554.6:p.Glu23137Asp
|
|
ENST00000359218.10:c.69210A>T
(TTN)
|
ENSP00000352154.5:p.Glu23070Asp
|
|
ENST00000342175.10:c.69411A>T
(TTN)
|
ENSP00000340554.6:p.Glu23137Asp
|
|
ENST00000342992.10:c.88326A>T
(TTN)
|
ENSP00000343764.6:p.Glu29442Asp
|
|
ENST00000359218.9:c.69210A>T
(TTN)
|
ENSP00000352154.5:p.Glu23070Asp
|
|
ENST00000460472.6:c.68835A>T
(TTN)
|
ENSP00000434586.1:p.Glu22945Asp
|
|
ENST00000589042.5:c.96030A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32010Asp
|
|
ENST00000591111.5:c.91107A>T
(TTN)
|
ENSP00000465570.1:p.Glu30369Asp
|
|
ENST00000615779.4:c.91107A>T
(TTN)
|
ENSP00000483597.1:p.Glu30369Asp
|
|
NM_001256850.1:c.91107A>T
(TTN)
|
NP_001243779.1:p.Glu30369Asp
|
|
NM_001267550.2:c.96030A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32010Asp
|
|
NM_003319.4:c.68835A>T
(TTN)
|
NP_003310.4:p.Glu22945Asp
|
|
NM_133378.4:c.88326A>T
(TTN)
|
NP_596869.4:p.Glu29442Asp
|
|
NM_133432.3:c.69210A>T
(TTN)
|
NP_597676.3:p.Glu23070Asp
|
|
NM_133437.4:c.69411A>T
(TTN)
|
NP_597681.4:p.Glu23137Asp
|
|
NR_038271.1:n.446+20478T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1753T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95127A>T
(TTN)
|
XP_011510031.1:p.Glu31709Asp
|
|
XM_011511730.1:c.69021A>T
(TTN)
|
XP_011510032.1:p.Glu23007Asp
|
|
XM_011511731.1:c.68880A>T
(TTN)
|
XP_011510033.1:p.Glu22960Asp
|
|
XM_017004819.1:c.94923A>T
(TTN)
|
XP_016860308.1:p.Glu31641Asp
|
|
XM_017004820.1:c.90321A>T
(TTN)
|
XP_016860309.1:p.Glu30107Asp
|
|
XM_017004821.1:c.90318A>T
(TTN)
|
XP_016860310.1:p.Glu30106Asp
|
|
XM_017004822.1:c.87360A>T
(TTN)
|
XP_016860311.1:p.Glu29120Asp
|
|
XM_017004823.1:c.68976A>T
(TTN)
|
XP_016860312.1:p.Glu22992Asp
|
|
XM_024453094.1:c.90471A>T
(TTN)
|
XP_024308862.1:p.Glu30157Asp
|
|
XM_024453095.1:c.90468A>T
(TTN)
|
XP_024308863.1:p.Glu30156Asp
|
|
XM_024453096.1:c.89901A>T
(TTN)
|
XP_024308864.1:p.Glu29967Asp
|
|
XM_024453097.1:c.87243A>T
(TTN)
|
XP_024308865.1:p.Glu29081Asp
|
|
XM_024453098.1:c.87162A>T
(TTN)
|
XP_024308866.1:p.Glu29054Asp
|
|
XM_024453099.1:c.68925A>T
(TTN)
|
XP_024308867.1:p.Glu22975Asp
|
|
XM_024453100.1:c.58779A>T
(TTN)
|
XP_024308868.1:p.Glu19593Asp
|
|