ENST00000342992.11:c.96686A>T
(TTN)
|
ENSP00000343764.6:p.Glu32229Val
|
|
ENST00000342175.11:c.77771A>T
(TTN)
|
ENSP00000340554.6:p.Glu25924Val
|
|
ENST00000359218.10:c.77570A>T
(TTN)
|
ENSP00000352154.5:p.Glu25857Val
|
|
ENST00000342175.10:c.77771A>T
(TTN)
|
ENSP00000340554.6:p.Glu25924Val
|
|
ENST00000342992.10:c.96686A>T
(TTN)
|
ENSP00000343764.6:p.Glu32229Val
|
|
ENST00000359218.9:c.77570A>T
(TTN)
|
ENSP00000352154.5:p.Glu25857Val
|
|
ENST00000460472.6:c.77195A>T
(TTN)
|
ENSP00000434586.1:p.Glu25732Val
|
|
ENST00000589042.5:c.104390A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34797Val
|
|
ENST00000591111.5:c.99467A>T
(TTN)
|
ENSP00000465570.1:p.Glu33156Val
|
|
ENST00000615779.4:c.99467A>T
(TTN)
|
ENSP00000483597.1:p.Glu33156Val
|
|
NM_001256850.1:c.99467A>T
(TTN)
|
NP_001243779.1:p.Glu33156Val
|
|
NM_001267550.2:c.104390A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34797Val
|
|
NM_003319.4:c.77195A>T
(TTN)
|
NP_003310.4:p.Glu25732Val
|
|
NM_133378.4:c.96686A>T
(TTN)
|
NP_596869.4:p.Glu32229Val
|
|
NM_133432.3:c.77570A>T
(TTN)
|
NP_597676.3:p.Glu25857Val
|
|
NM_133437.4:c.77771A>T
(TTN)
|
NP_597681.4:p.Glu25924Val
|
|
NR_038271.1:n.446+8589T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3507T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103487A>T
(TTN)
|
XP_011510031.1:p.Glu34496Val
|
|
XM_011511730.1:c.77381A>T
(TTN)
|
XP_011510032.1:p.Glu25794Val
|
|
XM_011511731.1:c.77240A>T
(TTN)
|
XP_011510033.1:p.Glu25747Val
|
|
XM_017004819.1:c.103283A>T
(TTN)
|
XP_016860308.1:p.Glu34428Val
|
|
XM_017004820.1:c.98681A>T
(TTN)
|
XP_016860309.1:p.Glu32894Val
|
|
XM_017004821.1:c.98678A>T
(TTN)
|
XP_016860310.1:p.Glu32893Val
|
|
XM_017004822.1:c.95720A>T
(TTN)
|
XP_016860311.1:p.Glu31907Val
|
|
XM_017004823.1:c.77336A>T
(TTN)
|
XP_016860312.1:p.Glu25779Val
|
|
XM_024453094.1:c.98831A>T
(TTN)
|
XP_024308862.1:p.Glu32944Val
|
|
XM_024453095.1:c.98828A>T
(TTN)
|
XP_024308863.1:p.Glu32943Val
|
|
XM_024453096.1:c.98261A>T
(TTN)
|
XP_024308864.1:p.Glu32754Val
|
|
XM_024453097.1:c.95603A>T
(TTN)
|
XP_024308865.1:p.Glu31868Val
|
|
XM_024453098.1:c.95522A>T
(TTN)
|
XP_024308866.1:p.Glu31841Val
|
|
XM_024453099.1:c.77285A>T
(TTN)
|
XP_024308867.1:p.Glu25762Val
|
|
XM_024453100.1:c.67139A>T
(TTN)
|
XP_024308868.1:p.Glu22380Val
|
|