ENST00000342992.11:c.100183A>G
(TTN)
|
ENSP00000343764.6:p.Lys33395Glu
|
|
ENST00000342175.11:c.81268A>G
(TTN)
|
ENSP00000340554.6:p.Lys27090Glu
|
|
ENST00000359218.10:c.81067A>G
(TTN)
|
ENSP00000352154.5:p.Lys27023Glu
|
|
ENST00000342175.10:c.81268A>G
(TTN)
|
ENSP00000340554.6:p.Lys27090Glu
|
|
ENST00000342992.10:c.100183A>G
(TTN)
|
ENSP00000343764.6:p.Lys33395Glu
|
|
ENST00000359218.9:c.81067A>G
(TTN)
|
ENSP00000352154.5:p.Lys27023Glu
|
|
ENST00000460472.6:c.80692A>G
(TTN)
|
ENSP00000434586.1:p.Lys26898Glu
|
|
ENST00000589042.5:c.107887A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys35963Glu
|
|
ENST00000591111.5:c.102964A>G
(TTN)
|
ENSP00000465570.1:p.Lys34322Glu
|
|
ENST00000615779.4:c.102964A>G
(TTN)
|
ENSP00000483597.1:p.Lys34322Glu
|
|
NM_001256850.1:c.102964A>G
(TTN)
|
NP_001243779.1:p.Lys34322Glu
|
|
NM_001267550.2:c.107887A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Lys35963Glu
|
|
NM_003319.4:c.80692A>G
(TTN)
|
NP_003310.4:p.Lys26898Glu
|
|
NM_133378.4:c.100183A>G
(TTN)
|
NP_596869.4:p.Lys33395Glu
|
|
NM_133432.3:c.81067A>G
(TTN)
|
NP_597676.3:p.Lys27023Glu
|
|
NM_133437.4:c.81268A>G
(TTN)
|
NP_597681.4:p.Lys27090Glu
|
|
NR_038271.1:n.446+3465T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3465T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.106984A>G
(TTN)
|
XP_011510031.1:p.Lys35662Glu
|
|
XM_011511730.1:c.80878A>G
(TTN)
|
XP_011510032.1:p.Lys26960Glu
|
|
XM_011511731.1:c.80737A>G
(TTN)
|
XP_011510033.1:p.Lys26913Glu
|
|
XM_017004819.1:c.106780A>G
(TTN)
|
XP_016860308.1:p.Lys35594Glu
|
|
XM_017004820.1:c.102178A>G
(TTN)
|
XP_016860309.1:p.Lys34060Glu
|
|
XM_017004821.1:c.102175A>G
(TTN)
|
XP_016860310.1:p.Lys34059Glu
|
|
XM_017004822.1:c.99217A>G
(TTN)
|
XP_016860311.1:p.Lys33073Glu
|
|
XM_017004823.1:c.80833A>G
(TTN)
|
XP_016860312.1:p.Lys26945Glu
|
|
XM_024453094.1:c.102328A>G
(TTN)
|
XP_024308862.1:p.Lys34110Glu
|
|
XM_024453095.1:c.102325A>G
(TTN)
|
XP_024308863.1:p.Lys34109Glu
|
|
XM_024453096.1:c.101758A>G
(TTN)
|
XP_024308864.1:p.Lys33920Glu
|
|
XM_024453097.1:c.99100A>G
(TTN)
|
XP_024308865.1:p.Lys33034Glu
|
|
XM_024453098.1:c.99019A>G
(TTN)
|
XP_024308866.1:p.Lys33007Glu
|
|
XM_024453099.1:c.80782A>G
(TTN)
|
XP_024308867.1:p.Lys26928Glu
|
|
XM_024453100.1:c.70636A>G
(TTN)
|
XP_024308868.1:p.Lys23546Glu
|
|