ENST00000342992.11:c.88340A>T
(TTN)
|
ENSP00000343764.6:p.Glu29447Val
|
|
ENST00000342175.11:c.69425A>T
(TTN)
|
ENSP00000340554.6:p.Glu23142Val
|
|
ENST00000359218.10:c.69224A>T
(TTN)
|
ENSP00000352154.5:p.Glu23075Val
|
|
ENST00000342175.10:c.69425A>T
(TTN)
|
ENSP00000340554.6:p.Glu23142Val
|
|
ENST00000342992.10:c.88340A>T
(TTN)
|
ENSP00000343764.6:p.Glu29447Val
|
|
ENST00000359218.9:c.69224A>T
(TTN)
|
ENSP00000352154.5:p.Glu23075Val
|
|
ENST00000460472.6:c.68849A>T
(TTN)
|
ENSP00000434586.1:p.Glu22950Val
|
|
ENST00000589042.5:c.96044A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32015Val
|
|
ENST00000591111.5:c.91121A>T
(TTN)
|
ENSP00000465570.1:p.Glu30374Val
|
|
ENST00000615779.4:c.91121A>T
(TTN)
|
ENSP00000483597.1:p.Glu30374Val
|
|
NM_001256850.1:c.91121A>T
(TTN)
|
NP_001243779.1:p.Glu30374Val
|
|
NM_001267550.2:c.96044A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32015Val
|
|
NM_003319.4:c.68849A>T
(TTN)
|
NP_003310.4:p.Glu22950Val
|
|
NM_133378.4:c.88340A>T
(TTN)
|
NP_596869.4:p.Glu29447Val
|
|
NM_133432.3:c.69224A>T
(TTN)
|
NP_597676.3:p.Glu23075Val
|
|
NM_133437.4:c.69425A>T
(TTN)
|
NP_597681.4:p.Glu23142Val
|
|
NR_038271.1:n.446+20464T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1739T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95141A>T
(TTN)
|
XP_011510031.1:p.Glu31714Val
|
|
XM_011511730.1:c.69035A>T
(TTN)
|
XP_011510032.1:p.Glu23012Val
|
|
XM_011511731.1:c.68894A>T
(TTN)
|
XP_011510033.1:p.Glu22965Val
|
|
XM_017004819.1:c.94937A>T
(TTN)
|
XP_016860308.1:p.Glu31646Val
|
|
XM_017004820.1:c.90335A>T
(TTN)
|
XP_016860309.1:p.Glu30112Val
|
|
XM_017004821.1:c.90332A>T
(TTN)
|
XP_016860310.1:p.Glu30111Val
|
|
XM_017004822.1:c.87374A>T
(TTN)
|
XP_016860311.1:p.Glu29125Val
|
|
XM_017004823.1:c.68990A>T
(TTN)
|
XP_016860312.1:p.Glu22997Val
|
|
XM_024453094.1:c.90485A>T
(TTN)
|
XP_024308862.1:p.Glu30162Val
|
|
XM_024453095.1:c.90482A>T
(TTN)
|
XP_024308863.1:p.Glu30161Val
|
|
XM_024453096.1:c.89915A>T
(TTN)
|
XP_024308864.1:p.Glu29972Val
|
|
XM_024453097.1:c.87257A>T
(TTN)
|
XP_024308865.1:p.Glu29086Val
|
|
XM_024453098.1:c.87176A>T
(TTN)
|
XP_024308866.1:p.Glu29059Val
|
|
XM_024453099.1:c.68939A>T
(TTN)
|
XP_024308867.1:p.Glu22980Val
|
|
XM_024453100.1:c.58793A>T
(TTN)
|
XP_024308868.1:p.Glu19598Val
|
|