ENST00000342992.11:c.69495T>C
(TTN)
|
ENSP00000343764.6:p.Tyr23165=
|
|
ENST00000342175.11:c.50580T>C
(TTN)
|
ENSP00000340554.6:p.Tyr16860=
|
|
ENST00000359218.10:c.50379T>C
(TTN)
|
ENSP00000352154.5:p.Tyr16793=
|
|
ENST00000342175.10:c.50580T>C
(TTN)
|
ENSP00000340554.6:p.Tyr16860=
|
|
ENST00000342992.10:c.69495T>C
(TTN)
|
ENSP00000343764.6:p.Tyr23165=
|
|
ENST00000359218.9:c.50379T>C
(TTN)
|
ENSP00000352154.5:p.Tyr16793=
|
|
ENST00000460472.6:c.50004T>C
(TTN)
|
ENSP00000434586.1:p.Tyr16668=
|
|
ENST00000589042.5:c.77199T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr25733=
|
|
ENST00000591111.5:c.72276T>C
(TTN)
|
ENSP00000465570.1:p.Tyr24092=
|
|
ENST00000615779.4:c.72276T>C
(TTN)
|
ENSP00000483597.1:p.Tyr24092=
|
|
NM_001256850.1:c.72276T>C
(TTN)
|
NP_001243779.1:p.Tyr24092=
|
|
NM_001267550.2:c.77199T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr25733=
|
|
NM_003319.4:c.50004T>C
(TTN)
|
NP_003310.4:p.Tyr16668=
|
|
NM_133378.4:c.69495T>C
(TTN)
|
NP_596869.4:p.Tyr23165=
|
|
NM_133432.3:c.50379T>C
(TTN)
|
NP_597676.3:p.Tyr16793=
|
|
NM_133437.4:c.50580T>C
(TTN)
|
NP_597681.4:p.Tyr16860=
|
|
NR_038271.1:n.447-2367A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13639A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.76296T>C
(TTN)
|
XP_011510031.1:p.Tyr25432=
|
|
XM_011511730.1:c.50190T>C
(TTN)
|
XP_011510032.1:p.Tyr16730=
|
|
XM_011511731.1:c.50049T>C
(TTN)
|
XP_011510033.1:p.Tyr16683=
|
|
XM_017004819.1:c.76092T>C
(TTN)
|
XP_016860308.1:p.Tyr25364=
|
|
XM_017004820.1:c.71490T>C
(TTN)
|
XP_016860309.1:p.Tyr23830=
|
|
XM_017004821.1:c.71487T>C
(TTN)
|
XP_016860310.1:p.Tyr23829=
|
|
XM_017004822.1:c.68529T>C
(TTN)
|
XP_016860311.1:p.Tyr22843=
|
|
XM_017004823.1:c.50145T>C
(TTN)
|
XP_016860312.1:p.Tyr16715=
|
|
XM_024453094.1:c.71640T>C
(TTN)
|
XP_024308862.1:p.Tyr23880=
|
|
XM_024453095.1:c.71637T>C
(TTN)
|
XP_024308863.1:p.Tyr23879=
|
|
XM_024453096.1:c.71070T>C
(TTN)
|
XP_024308864.1:p.Tyr23690=
|
|
XM_024453097.1:c.68412T>C
(TTN)
|
XP_024308865.1:p.Tyr22804=
|
|
XM_024453098.1:c.68331T>C
(TTN)
|
XP_024308866.1:p.Tyr22777=
|
|
XM_024453099.1:c.50094T>C
(TTN)
|
XP_024308867.1:p.Tyr16698=
|
|
XM_024453100.1:c.39948T>C
(TTN)
|
XP_024308868.1:p.Tyr13316=
|
|