ENST00000342992.11:c.78687T>G
(TTN)
|
ENSP00000343764.6:p.Thr26229=
|
|
ENST00000342175.11:c.59772T>G
(TTN)
|
ENSP00000340554.6:p.Thr19924=
|
|
ENST00000359218.10:c.59571T>G
(TTN)
|
ENSP00000352154.5:p.Thr19857=
|
|
ENST00000342175.10:c.59772T>G
(TTN)
|
ENSP00000340554.6:p.Thr19924=
|
|
ENST00000342992.10:c.78687T>G
(TTN)
|
ENSP00000343764.6:p.Thr26229=
|
|
ENST00000359218.9:c.59571T>G
(TTN)
|
ENSP00000352154.5:p.Thr19857=
|
|
ENST00000460472.6:c.59196T>G
(TTN)
|
ENSP00000434586.1:p.Thr19732=
|
|
ENST00000589042.5:c.86391T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr28797=
|
|
ENST00000591111.5:c.81468T>G
(TTN)
|
ENSP00000465570.1:p.Thr27156=
|
|
ENST00000615779.4:c.81468T>G
(TTN)
|
ENSP00000483597.1:p.Thr27156=
|
|
NM_001256850.1:c.81468T>G
(TTN)
|
NP_001243779.1:p.Thr27156=
|
|
NM_001267550.2:c.86391T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr28797=
|
|
NM_003319.4:c.59196T>G
(TTN)
|
NP_003310.4:p.Thr19732=
|
|
NM_133378.4:c.78687T>G
(TTN)
|
NP_596869.4:p.Thr26229=
|
|
NM_133432.3:c.59571T>G
(TTN)
|
NP_597676.3:p.Thr19857=
|
|
NM_133437.4:c.59772T>G
(TTN)
|
NP_597681.4:p.Thr19924=
|
|
NR_038271.1:n.447-11559A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17380A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85488T>G
(TTN)
|
XP_011510031.1:p.Thr28496=
|
|
XM_011511730.1:c.59382T>G
(TTN)
|
XP_011510032.1:p.Thr19794=
|
|
XM_011511731.1:c.59241T>G
(TTN)
|
XP_011510033.1:p.Thr19747=
|
|
XM_017004819.1:c.85284T>G
(TTN)
|
XP_016860308.1:p.Thr28428=
|
|
XM_017004820.1:c.80682T>G
(TTN)
|
XP_016860309.1:p.Thr26894=
|
|
XM_017004821.1:c.80679T>G
(TTN)
|
XP_016860310.1:p.Thr26893=
|
|
XM_017004822.1:c.77721T>G
(TTN)
|
XP_016860311.1:p.Thr25907=
|
|
XM_017004823.1:c.59337T>G
(TTN)
|
XP_016860312.1:p.Thr19779=
|
|
XM_024453094.1:c.80832T>G
(TTN)
|
XP_024308862.1:p.Thr26944=
|
|
XM_024453095.1:c.80829T>G
(TTN)
|
XP_024308863.1:p.Thr26943=
|
|
XM_024453096.1:c.80262T>G
(TTN)
|
XP_024308864.1:p.Thr26754=
|
|
XM_024453097.1:c.77604T>G
(TTN)
|
XP_024308865.1:p.Thr25868=
|
|
XM_024453098.1:c.77523T>G
(TTN)
|
XP_024308866.1:p.Thr25841=
|
|
XM_024453099.1:c.59286T>G
(TTN)
|
XP_024308867.1:p.Thr19762=
|
|
XM_024453100.1:c.49140T>G
(TTN)
|
XP_024308868.1:p.Thr16380=
|
|