ENST00000342992.11:c.96722T>G
(TTN)
|
ENSP00000343764.6:p.Val32241Gly
|
|
ENST00000342175.11:c.77807T>G
(TTN)
|
ENSP00000340554.6:p.Val25936Gly
|
|
ENST00000359218.10:c.77606T>G
(TTN)
|
ENSP00000352154.5:p.Val25869Gly
|
|
ENST00000342175.10:c.77807T>G
(TTN)
|
ENSP00000340554.6:p.Val25936Gly
|
|
ENST00000342992.10:c.96722T>G
(TTN)
|
ENSP00000343764.6:p.Val32241Gly
|
|
ENST00000359218.9:c.77606T>G
(TTN)
|
ENSP00000352154.5:p.Val25869Gly
|
|
ENST00000460472.6:c.77231T>G
(TTN)
|
ENSP00000434586.1:p.Val25744Gly
|
|
ENST00000589042.5:c.104426T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val34809Gly
|
|
ENST00000591111.5:c.99503T>G
(TTN)
|
ENSP00000465570.1:p.Val33168Gly
|
|
ENST00000615779.4:c.99503T>G
(TTN)
|
ENSP00000483597.1:p.Val33168Gly
|
|
NM_001256850.1:c.99503T>G
(TTN)
|
NP_001243779.1:p.Val33168Gly
|
|
NM_001267550.2:c.104426T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val34809Gly
|
|
NM_003319.4:c.77231T>G
(TTN)
|
NP_003310.4:p.Val25744Gly
|
|
NM_133378.4:c.96722T>G
(TTN)
|
NP_596869.4:p.Val32241Gly
|
|
NM_133432.3:c.77606T>G
(TTN)
|
NP_597676.3:p.Val25869Gly
|
|
NM_133437.4:c.77807T>G
(TTN)
|
NP_597681.4:p.Val25936Gly
|
|
NR_038271.1:n.446+8553A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3543A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103523T>G
(TTN)
|
XP_011510031.1:p.Val34508Gly
|
|
XM_011511730.1:c.77417T>G
(TTN)
|
XP_011510032.1:p.Val25806Gly
|
|
XM_011511731.1:c.77276T>G
(TTN)
|
XP_011510033.1:p.Val25759Gly
|
|
XM_017004819.1:c.103319T>G
(TTN)
|
XP_016860308.1:p.Val34440Gly
|
|
XM_017004820.1:c.98717T>G
(TTN)
|
XP_016860309.1:p.Val32906Gly
|
|
XM_017004821.1:c.98714T>G
(TTN)
|
XP_016860310.1:p.Val32905Gly
|
|
XM_017004822.1:c.95756T>G
(TTN)
|
XP_016860311.1:p.Val31919Gly
|
|
XM_017004823.1:c.77372T>G
(TTN)
|
XP_016860312.1:p.Val25791Gly
|
|
XM_024453094.1:c.98867T>G
(TTN)
|
XP_024308862.1:p.Val32956Gly
|
|
XM_024453095.1:c.98864T>G
(TTN)
|
XP_024308863.1:p.Val32955Gly
|
|
XM_024453096.1:c.98297T>G
(TTN)
|
XP_024308864.1:p.Val32766Gly
|
|
XM_024453097.1:c.95639T>G
(TTN)
|
XP_024308865.1:p.Val31880Gly
|
|
XM_024453098.1:c.95558T>G
(TTN)
|
XP_024308866.1:p.Val31853Gly
|
|
XM_024453099.1:c.77321T>G
(TTN)
|
XP_024308867.1:p.Val25774Gly
|
|
XM_024453100.1:c.67175T>G
(TTN)
|
XP_024308868.1:p.Val22392Gly
|
|