ENST00000342992.11:c.54606A>T
(TTN)
|
ENSP00000343764.6:p.Val18202=
|
|
ENST00000342175.11:c.35691A>T
(TTN)
|
ENSP00000340554.6:p.Val11897=
|
|
ENST00000359218.10:c.35490A>T
(TTN)
|
ENSP00000352154.5:p.Val11830=
|
|
ENST00000342175.10:c.35691A>T
(TTN)
|
ENSP00000340554.6:p.Val11897=
|
|
ENST00000342992.10:c.54606A>T
(TTN)
|
ENSP00000343764.6:p.Val18202=
|
|
ENST00000359218.9:c.35490A>T
(TTN)
|
ENSP00000352154.5:p.Val11830=
|
|
ENST00000460472.6:c.35115A>T
(TTN)
|
ENSP00000434586.1:p.Val11705=
|
|
ENST00000589042.5:c.62310A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val20770=
|
|
ENST00000591111.5:c.57387A>T
(TTN)
|
ENSP00000465570.1:p.Val19129=
|
|
ENST00000615779.4:c.57387A>T
(TTN)
|
ENSP00000483597.1:p.Val19129=
|
|
NM_001256850.1:c.57387A>T
(TTN)
|
NP_001243779.1:p.Val19129=
|
|
NM_001267550.2:c.62310A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Val20770=
|
|
NM_003319.4:c.35115A>T
(TTN)
|
NP_003310.4:p.Val11705=
|
|
NM_133378.4:c.54606A>T
(TTN)
|
NP_596869.4:p.Val18202=
|
|
NM_133432.3:c.35490A>T
(TTN)
|
NP_597676.3:p.Val11830=
|
|
NM_133437.4:c.35691A>T
(TTN)
|
NP_597681.4:p.Val11897=
|
|
NR_038271.1:n.597-8181T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-1724T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.61407A>T
(TTN)
|
XP_011510031.1:p.Val20469=
|
|
XM_011511730.1:c.35301A>T
(TTN)
|
XP_011510032.1:p.Val11767=
|
|
XM_011511731.1:c.35160A>T
(TTN)
|
XP_011510033.1:p.Val11720=
|
|
XM_017004819.1:c.61203A>T
(TTN)
|
XP_016860308.1:p.Val20401=
|
|
XM_017004820.1:c.56601A>T
(TTN)
|
XP_016860309.1:p.Val18867=
|
|
XM_017004821.1:c.56598A>T
(TTN)
|
XP_016860310.1:p.Val18866=
|
|
XM_017004822.1:c.53640A>T
(TTN)
|
XP_016860311.1:p.Val17880=
|
|
XM_017004823.1:c.35256A>T
(TTN)
|
XP_016860312.1:p.Val11752=
|
|
XM_024453094.1:c.56751A>T
(TTN)
|
XP_024308862.1:p.Val18917=
|
|
XM_024453095.1:c.56748A>T
(TTN)
|
XP_024308863.1:p.Val18916=
|
|
XM_024453096.1:c.56181A>T
(TTN)
|
XP_024308864.1:p.Val18727=
|
|
XM_024453097.1:c.53523A>T
(TTN)
|
XP_024308865.1:p.Val17841=
|
|
XM_024453098.1:c.53442A>T
(TTN)
|
XP_024308866.1:p.Val17814=
|
|
XM_024453099.1:c.35205A>T
(TTN)
|
XP_024308867.1:p.Val11735=
|
|
XM_024453100.1:c.25059A>T
(TTN)
|
XP_024308868.1:p.Val8353=
|
|