ENST00000342992.11:c.88301A>T
(TTN)
|
ENSP00000343764.6:p.Glu29434Val
|
|
ENST00000342175.11:c.69386A>T
(TTN)
|
ENSP00000340554.6:p.Glu23129Val
|
|
ENST00000359218.10:c.69185A>T
(TTN)
|
ENSP00000352154.5:p.Glu23062Val
|
|
ENST00000342175.10:c.69386A>T
(TTN)
|
ENSP00000340554.6:p.Glu23129Val
|
|
ENST00000342992.10:c.88301A>T
(TTN)
|
ENSP00000343764.6:p.Glu29434Val
|
|
ENST00000359218.9:c.69185A>T
(TTN)
|
ENSP00000352154.5:p.Glu23062Val
|
|
ENST00000460472.6:c.68810A>T
(TTN)
|
ENSP00000434586.1:p.Glu22937Val
|
|
ENST00000589042.5:c.96005A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32002Val
|
|
ENST00000591111.5:c.91082A>T
(TTN)
|
ENSP00000465570.1:p.Glu30361Val
|
|
ENST00000615779.4:c.91082A>T
(TTN)
|
ENSP00000483597.1:p.Glu30361Val
|
|
NM_001256850.1:c.91082A>T
(TTN)
|
NP_001243779.1:p.Glu30361Val
|
|
NM_001267550.2:c.96005A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32002Val
|
|
NM_003319.4:c.68810A>T
(TTN)
|
NP_003310.4:p.Glu22937Val
|
|
NM_133378.4:c.88301A>T
(TTN)
|
NP_596869.4:p.Glu29434Val
|
|
NM_133432.3:c.69185A>T
(TTN)
|
NP_597676.3:p.Glu23062Val
|
|
NM_133437.4:c.69386A>T
(TTN)
|
NP_597681.4:p.Glu23129Val
|
|
NR_038271.1:n.446+20588T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1863T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95102A>T
(TTN)
|
XP_011510031.1:p.Glu31701Val
|
|
XM_011511730.1:c.68996A>T
(TTN)
|
XP_011510032.1:p.Glu22999Val
|
|
XM_011511731.1:c.68855A>T
(TTN)
|
XP_011510033.1:p.Glu22952Val
|
|
XM_017004819.1:c.94898A>T
(TTN)
|
XP_016860308.1:p.Glu31633Val
|
|
XM_017004820.1:c.90296A>T
(TTN)
|
XP_016860309.1:p.Glu30099Val
|
|
XM_017004821.1:c.90293A>T
(TTN)
|
XP_016860310.1:p.Glu30098Val
|
|
XM_017004822.1:c.87335A>T
(TTN)
|
XP_016860311.1:p.Glu29112Val
|
|
XM_017004823.1:c.68951A>T
(TTN)
|
XP_016860312.1:p.Glu22984Val
|
|
XM_024453094.1:c.90446A>T
(TTN)
|
XP_024308862.1:p.Glu30149Val
|
|
XM_024453095.1:c.90443A>T
(TTN)
|
XP_024308863.1:p.Glu30148Val
|
|
XM_024453096.1:c.89876A>T
(TTN)
|
XP_024308864.1:p.Glu29959Val
|
|
XM_024453097.1:c.87218A>T
(TTN)
|
XP_024308865.1:p.Glu29073Val
|
|
XM_024453098.1:c.87137A>T
(TTN)
|
XP_024308866.1:p.Glu29046Val
|
|
XM_024453099.1:c.68900A>T
(TTN)
|
XP_024308867.1:p.Glu22967Val
|
|
XM_024453100.1:c.58754A>T
(TTN)
|
XP_024308868.1:p.Glu19585Val
|
|