ENST00000342992.11:c.50655T>A
(TTN)
|
ENSP00000343764.6:p.Asp16885Glu
|
|
ENST00000342175.11:c.31740T>A
(TTN)
|
ENSP00000340554.6:p.Asp10580Glu
|
|
ENST00000359218.10:c.31539T>A
(TTN)
|
ENSP00000352154.5:p.Asp10513Glu
|
|
ENST00000342175.10:c.31740T>A
(TTN)
|
ENSP00000340554.6:p.Asp10580Glu
|
|
ENST00000342992.10:c.50655T>A
(TTN)
|
ENSP00000343764.6:p.Asp16885Glu
|
|
ENST00000359218.9:c.31539T>A
(TTN)
|
ENSP00000352154.5:p.Asp10513Glu
|
|
ENST00000460472.6:c.31164T>A
(TTN)
|
ENSP00000434586.1:p.Asp10388Glu
|
|
ENST00000589042.5:c.58359T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19453Glu
|
|
ENST00000591111.5:c.53436T>A
(TTN)
|
ENSP00000465570.1:p.Asp17812Glu
|
|
ENST00000615779.4:c.53436T>A
(TTN)
|
ENSP00000483597.1:p.Asp17812Glu
|
|
NM_001256850.1:c.53436T>A
(TTN)
|
NP_001243779.1:p.Asp17812Glu
|
|
NM_001267550.2:c.58359T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19453Glu
|
|
NM_003319.4:c.31164T>A
(TTN)
|
NP_003310.4:p.Asp10388Glu
|
|
NM_133378.4:c.50655T>A
(TTN)
|
NP_596869.4:p.Asp16885Glu
|
|
NM_133432.3:c.31539T>A
(TTN)
|
NP_597676.3:p.Asp10513Glu
|
|
NM_133437.4:c.31740T>A
(TTN)
|
NP_597681.4:p.Asp10580Glu
|
|
NR_038271.1:n.597-3562A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+2720A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.57456T>A
(TTN)
|
XP_011510031.1:p.Asp19152Glu
|
|
XM_011511730.1:c.31350T>A
(TTN)
|
XP_011510032.1:p.Asp10450Glu
|
|
XM_011511731.1:c.31209T>A
(TTN)
|
XP_011510033.1:p.Asp10403Glu
|
|
XM_017004819.1:c.57252T>A
(TTN)
|
XP_016860308.1:p.Asp19084Glu
|
|
XM_017004820.1:c.52650T>A
(TTN)
|
XP_016860309.1:p.Asp17550Glu
|
|
XM_017004821.1:c.52647T>A
(TTN)
|
XP_016860310.1:p.Asp17549Glu
|
|
XM_017004822.1:c.49689T>A
(TTN)
|
XP_016860311.1:p.Asp16563Glu
|
|
XM_017004823.1:c.31305T>A
(TTN)
|
XP_016860312.1:p.Asp10435Glu
|
|
XM_024453094.1:c.52800T>A
(TTN)
|
XP_024308862.1:p.Asp17600Glu
|
|
XM_024453095.1:c.52797T>A
(TTN)
|
XP_024308863.1:p.Asp17599Glu
|
|
XM_024453096.1:c.52230T>A
(TTN)
|
XP_024308864.1:p.Asp17410Glu
|
|
XM_024453097.1:c.49572T>A
(TTN)
|
XP_024308865.1:p.Asp16524Glu
|
|
XM_024453098.1:c.49491T>A
(TTN)
|
XP_024308866.1:p.Asp16497Glu
|
|
XM_024453099.1:c.31254T>A
(TTN)
|
XP_024308867.1:p.Asp10418Glu
|
|
XM_024453100.1:c.21108T>A
(TTN)
|
XP_024308868.1:p.Asp7036Glu
|
|