|
ENST00000342992.11:c.62713G>T
(TTN)
|
ENSP00000343764.6:p.Glu20905Ter
|
|
|
ENST00000342175.11:c.43798G>T
(TTN)
|
ENSP00000340554.6:p.Glu14600Ter
|
|
|
ENST00000359218.10:c.43597G>T
(TTN)
|
ENSP00000352154.5:p.Glu14533Ter
|
|
|
ENST00000342175.10:c.43798G>T
(TTN)
|
ENSP00000340554.6:p.Glu14600Ter
|
|
|
ENST00000342992.10:c.62713G>T
(TTN)
|
ENSP00000343764.6:p.Glu20905Ter
|
|
|
ENST00000359218.9:c.43597G>T
(TTN)
|
ENSP00000352154.5:p.Glu14533Ter
|
|
|
ENST00000460472.6:c.43222G>T
(TTN)
|
ENSP00000434586.1:p.Glu14408Ter
|
|
|
ENST00000589042.5:c.70417G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu23473Ter
|
|
|
ENST00000591111.5:c.65494G>T
(TTN)
|
ENSP00000465570.1:p.Glu21832Ter
|
|
|
ENST00000615779.4:c.65494G>T
(TTN)
|
ENSP00000483597.1:p.Glu21832Ter
|
|
|
NM_001256850.1:c.65494G>T
(TTN)
|
NP_001243779.1:p.Glu21832Ter
|
|
|
NM_001267550.2:c.70417G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu23473Ter
|
|
|
NM_003319.4:c.43222G>T
(TTN)
|
NP_003310.4:p.Glu14408Ter
|
|
|
NM_133378.4:c.62713G>T
(TTN)
|
NP_596869.4:p.Glu20905Ter
|
|
|
NM_133432.3:c.43597G>T
(TTN)
|
NP_597676.3:p.Glu14533Ter
|
|
|
NM_133437.4:c.43798G>T
(TTN)
|
NP_597681.4:p.Glu14600Ter
|
|
|
NR_038271.1:n.596+4266C>A
(TTN-AS1)
|
|
|
|
NR_038272.1:n.2044-6857C>A
(TTN-AS1)
|
|
|
|
XM_011511729.1:c.69514G>T
(TTN)
|
XP_011510031.1:p.Glu23172Ter
|
|
|
XM_011511730.1:c.43408G>T
(TTN)
|
XP_011510032.1:p.Glu14470Ter
|
|
|
XM_011511731.1:c.43267G>T
(TTN)
|
XP_011510033.1:p.Glu14423Ter
|
|
|
XM_017004819.1:c.69310G>T
(TTN)
|
XP_016860308.1:p.Glu23104Ter
|
|
|
XM_017004820.1:c.64708G>T
(TTN)
|
XP_016860309.1:p.Glu21570Ter
|
|
|
XM_017004821.1:c.64705G>T
(TTN)
|
XP_016860310.1:p.Glu21569Ter
|
|
|
XM_017004822.1:c.61747G>T
(TTN)
|
XP_016860311.1:p.Glu20583Ter
|
|
|
XM_017004823.1:c.43363G>T
(TTN)
|
XP_016860312.1:p.Glu14455Ter
|
|
|
XM_024453094.1:c.64858G>T
(TTN)
|
XP_024308862.1:p.Glu21620Ter
|
|
|
XM_024453095.1:c.64855G>T
(TTN)
|
XP_024308863.1:p.Glu21619Ter
|
|
|
XM_024453096.1:c.64288G>T
(TTN)
|
XP_024308864.1:p.Glu21430Ter
|
|
|
XM_024453097.1:c.61630G>T
(TTN)
|
XP_024308865.1:p.Glu20544Ter
|
|
|
XM_024453098.1:c.61549G>T
(TTN)
|
XP_024308866.1:p.Glu20517Ter
|
|
|
XM_024453099.1:c.43312G>T
(TTN)
|
XP_024308867.1:p.Glu14438Ter
|
|
|
XM_024453100.1:c.33166G>T
(TTN)
|
XP_024308868.1:p.Glu11056Ter
|
|
