ENST00000342992.11:c.52244A>G
(TTN)
|
ENSP00000343764.6:p.Asp17415Gly
|
|
ENST00000342175.11:c.33329A>G
(TTN)
|
ENSP00000340554.6:p.Asp11110Gly
|
|
ENST00000359218.10:c.33128A>G
(TTN)
|
ENSP00000352154.5:p.Asp11043Gly
|
|
ENST00000342175.10:c.33329A>G
(TTN)
|
ENSP00000340554.6:p.Asp11110Gly
|
|
ENST00000342992.10:c.52244A>G
(TTN)
|
ENSP00000343764.6:p.Asp17415Gly
|
|
ENST00000359218.9:c.33128A>G
(TTN)
|
ENSP00000352154.5:p.Asp11043Gly
|
|
ENST00000460472.6:c.32753A>G
(TTN)
|
ENSP00000434586.1:p.Asp10918Gly
|
|
ENST00000589042.5:c.59948A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp19983Gly
|
|
ENST00000591111.5:c.55025A>G
(TTN)
|
ENSP00000465570.1:p.Asp18342Gly
|
|
ENST00000615779.4:c.55025A>G
(TTN)
|
ENSP00000483597.1:p.Asp18342Gly
|
|
NM_001256850.1:c.55025A>G
(TTN)
|
NP_001243779.1:p.Asp18342Gly
|
|
NM_001267550.2:c.59948A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp19983Gly
|
|
NM_003319.4:c.32753A>G
(TTN)
|
NP_003310.4:p.Asp10918Gly
|
|
NM_133378.4:c.52244A>G
(TTN)
|
NP_596869.4:p.Asp17415Gly
|
|
NM_133432.3:c.33128A>G
(TTN)
|
NP_597676.3:p.Asp11043Gly
|
|
NM_133437.4:c.33329A>G
(TTN)
|
NP_597681.4:p.Asp11110Gly
|
|
NR_038271.1:n.597-5725T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+557T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59045A>G
(TTN)
|
XP_011510031.1:p.Asp19682Gly
|
|
XM_011511730.1:c.32939A>G
(TTN)
|
XP_011510032.1:p.Asp10980Gly
|
|
XM_011511731.1:c.32798A>G
(TTN)
|
XP_011510033.1:p.Asp10933Gly
|
|
XM_017004819.1:c.58841A>G
(TTN)
|
XP_016860308.1:p.Asp19614Gly
|
|
XM_017004820.1:c.54239A>G
(TTN)
|
XP_016860309.1:p.Asp18080Gly
|
|
XM_017004821.1:c.54236A>G
(TTN)
|
XP_016860310.1:p.Asp18079Gly
|
|
XM_017004822.1:c.51278A>G
(TTN)
|
XP_016860311.1:p.Asp17093Gly
|
|
XM_017004823.1:c.32894A>G
(TTN)
|
XP_016860312.1:p.Asp10965Gly
|
|
XM_024453094.1:c.54389A>G
(TTN)
|
XP_024308862.1:p.Asp18130Gly
|
|
XM_024453095.1:c.54386A>G
(TTN)
|
XP_024308863.1:p.Asp18129Gly
|
|
XM_024453096.1:c.53819A>G
(TTN)
|
XP_024308864.1:p.Asp17940Gly
|
|
XM_024453097.1:c.51161A>G
(TTN)
|
XP_024308865.1:p.Asp17054Gly
|
|
XM_024453098.1:c.51080A>G
(TTN)
|
XP_024308866.1:p.Asp17027Gly
|
|
XM_024453099.1:c.32843A>G
(TTN)
|
XP_024308867.1:p.Asp10948Gly
|
|
XM_024453100.1:c.22697A>G
(TTN)
|
XP_024308868.1:p.Asp7566Gly
|
|