ENST00000342992.11:c.88202A>T
(TTN)
|
ENSP00000343764.6:p.Glu29401Val
|
|
ENST00000342175.11:c.69287A>T
(TTN)
|
ENSP00000340554.6:p.Glu23096Val
|
|
ENST00000359218.10:c.69086A>T
(TTN)
|
ENSP00000352154.5:p.Glu23029Val
|
|
ENST00000342175.10:c.69287A>T
(TTN)
|
ENSP00000340554.6:p.Glu23096Val
|
|
ENST00000342992.10:c.88202A>T
(TTN)
|
ENSP00000343764.6:p.Glu29401Val
|
|
ENST00000359218.9:c.69086A>T
(TTN)
|
ENSP00000352154.5:p.Glu23029Val
|
|
ENST00000460472.6:c.68711A>T
(TTN)
|
ENSP00000434586.1:p.Glu22904Val
|
|
ENST00000589042.5:c.95906A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu31969Val
|
|
ENST00000591111.5:c.90983A>T
(TTN)
|
ENSP00000465570.1:p.Glu30328Val
|
|
ENST00000615779.4:c.90983A>T
(TTN)
|
ENSP00000483597.1:p.Glu30328Val
|
|
NM_001256850.1:c.90983A>T
(TTN)
|
NP_001243779.1:p.Glu30328Val
|
|
NM_001267550.2:c.95906A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu31969Val
|
|
NM_003319.4:c.68711A>T
(TTN)
|
NP_003310.4:p.Glu22904Val
|
|
NM_133378.4:c.88202A>T
(TTN)
|
NP_596869.4:p.Glu29401Val
|
|
NM_133432.3:c.69086A>T
(TTN)
|
NP_597676.3:p.Glu23029Val
|
|
NM_133437.4:c.69287A>T
(TTN)
|
NP_597681.4:p.Glu23096Val
|
|
NR_038271.1:n.446+20687T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1962T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.95003A>T
(TTN)
|
XP_011510031.1:p.Glu31668Val
|
|
XM_011511730.1:c.68897A>T
(TTN)
|
XP_011510032.1:p.Glu22966Val
|
|
XM_011511731.1:c.68756A>T
(TTN)
|
XP_011510033.1:p.Glu22919Val
|
|
XM_017004819.1:c.94799A>T
(TTN)
|
XP_016860308.1:p.Glu31600Val
|
|
XM_017004820.1:c.90197A>T
(TTN)
|
XP_016860309.1:p.Glu30066Val
|
|
XM_017004821.1:c.90194A>T
(TTN)
|
XP_016860310.1:p.Glu30065Val
|
|
XM_017004822.1:c.87236A>T
(TTN)
|
XP_016860311.1:p.Glu29079Val
|
|
XM_017004823.1:c.68852A>T
(TTN)
|
XP_016860312.1:p.Glu22951Val
|
|
XM_024453094.1:c.90347A>T
(TTN)
|
XP_024308862.1:p.Glu30116Val
|
|
XM_024453095.1:c.90344A>T
(TTN)
|
XP_024308863.1:p.Glu30115Val
|
|
XM_024453096.1:c.89777A>T
(TTN)
|
XP_024308864.1:p.Glu29926Val
|
|
XM_024453097.1:c.87119A>T
(TTN)
|
XP_024308865.1:p.Glu29040Val
|
|
XM_024453098.1:c.87038A>T
(TTN)
|
XP_024308866.1:p.Glu29013Val
|
|
XM_024453099.1:c.68801A>T
(TTN)
|
XP_024308867.1:p.Glu22934Val
|
|
XM_024453100.1:c.58655A>T
(TTN)
|
XP_024308868.1:p.Glu19552Val
|
|