ENST00000342992.11:c.62458C>G
(TTN)
|
ENSP00000343764.6:p.Arg20820Gly
|
|
ENST00000342175.11:c.43543C>G
(TTN)
|
ENSP00000340554.6:p.Arg14515Gly
|
|
ENST00000359218.10:c.43342C>G
(TTN)
|
ENSP00000352154.5:p.Arg14448Gly
|
|
ENST00000342175.10:c.43543C>G
(TTN)
|
ENSP00000340554.6:p.Arg14515Gly
|
|
ENST00000342992.10:c.62458C>G
(TTN)
|
ENSP00000343764.6:p.Arg20820Gly
|
|
ENST00000359218.9:c.43342C>G
(TTN)
|
ENSP00000352154.5:p.Arg14448Gly
|
|
ENST00000460472.6:c.42967C>G
(TTN)
|
ENSP00000434586.1:p.Arg14323Gly
|
|
ENST00000589042.5:c.70162C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg23388Gly
|
|
ENST00000591111.5:c.65239C>G
(TTN)
|
ENSP00000465570.1:p.Arg21747Gly
|
|
ENST00000615779.4:c.65239C>G
(TTN)
|
ENSP00000483597.1:p.Arg21747Gly
|
|
NM_001256850.1:c.65239C>G
(TTN)
|
NP_001243779.1:p.Arg21747Gly
|
|
NM_001267550.2:c.70162C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Arg23388Gly
|
|
NM_003319.4:c.42967C>G
(TTN)
|
NP_003310.4:p.Arg14323Gly
|
|
NM_133378.4:c.62458C>G
(TTN)
|
NP_596869.4:p.Arg20820Gly
|
|
NM_133432.3:c.43342C>G
(TTN)
|
NP_597676.3:p.Arg14448Gly
|
|
NM_133437.4:c.43543C>G
(TTN)
|
NP_597681.4:p.Arg14515Gly
|
|
NR_038271.1:n.596+4521G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-6602G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.69259C>G
(TTN)
|
XP_011510031.1:p.Arg23087Gly
|
|
XM_011511730.1:c.43153C>G
(TTN)
|
XP_011510032.1:p.Arg14385Gly
|
|
XM_011511731.1:c.43012C>G
(TTN)
|
XP_011510033.1:p.Arg14338Gly
|
|
XM_017004819.1:c.69055C>G
(TTN)
|
XP_016860308.1:p.Arg23019Gly
|
|
XM_017004820.1:c.64453C>G
(TTN)
|
XP_016860309.1:p.Arg21485Gly
|
|
XM_017004821.1:c.64450C>G
(TTN)
|
XP_016860310.1:p.Arg21484Gly
|
|
XM_017004822.1:c.61492C>G
(TTN)
|
XP_016860311.1:p.Arg20498Gly
|
|
XM_017004823.1:c.43108C>G
(TTN)
|
XP_016860312.1:p.Arg14370Gly
|
|
XM_024453094.1:c.64603C>G
(TTN)
|
XP_024308862.1:p.Arg21535Gly
|
|
XM_024453095.1:c.64600C>G
(TTN)
|
XP_024308863.1:p.Arg21534Gly
|
|
XM_024453096.1:c.64033C>G
(TTN)
|
XP_024308864.1:p.Arg21345Gly
|
|
XM_024453097.1:c.61375C>G
(TTN)
|
XP_024308865.1:p.Arg20459Gly
|
|
XM_024453098.1:c.61294C>G
(TTN)
|
XP_024308866.1:p.Arg20432Gly
|
|
XM_024453099.1:c.43057C>G
(TTN)
|
XP_024308867.1:p.Arg14353Gly
|
|
XM_024453100.1:c.32911C>G
(TTN)
|
XP_024308868.1:p.Arg10971Gly
|
|