ENST00000342992.11:c.39068A>G
(TTN)
|
ENSP00000343764.6:p.Tyr13023Cys
|
|
ENST00000342175.11:c.20153A>G
(TTN)
|
ENSP00000340554.6:p.Tyr6718Cys
|
|
ENST00000359218.10:c.19952A>G
(TTN)
|
ENSP00000352154.5:p.Tyr6651Cys
|
|
ENST00000342175.10:c.20153A>G
(TTN)
|
ENSP00000340554.6:p.Tyr6718Cys
|
|
ENST00000342992.10:c.39068A>G
(TTN)
|
ENSP00000343764.6:p.Tyr13023Cys
|
|
ENST00000359218.9:c.19952A>G
(TTN)
|
ENSP00000352154.5:p.Tyr6651Cys
|
|
ENST00000460472.6:c.19577A>G
(TTN)
|
ENSP00000434586.1:p.Tyr6526Cys
|
|
ENST00000589042.5:c.46772A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr15591Cys
|
|
ENST00000591111.5:c.41849A>G
(TTN)
|
ENSP00000465570.1:p.Tyr13950Cys
|
|
ENST00000615779.4:c.41849A>G
(TTN)
|
ENSP00000483597.1:p.Tyr13950Cys
|
|
NM_001256850.1:c.41849A>G
(TTN)
|
NP_001243779.1:p.Tyr13950Cys
|
|
NM_001267550.2:c.46772A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr15591Cys
|
|
NM_003319.4:c.19577A>G
(TTN)
|
NP_003310.4:p.Tyr6526Cys
|
|
NM_133378.4:c.39068A>G
(TTN)
|
NP_596869.4:p.Tyr13023Cys
|
|
NM_133432.3:c.19952A>G
(TTN)
|
NP_597676.3:p.Tyr6651Cys
|
|
NM_133437.4:c.20153A>G
(TTN)
|
NP_597681.4:p.Tyr6718Cys
|
|
NR_038271.1:n.1605-975T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.45869A>G
(TTN)
|
XP_011510031.1:p.Tyr15290Cys
|
|
XM_011511730.1:c.19763A>G
(TTN)
|
XP_011510032.1:p.Tyr6588Cys
|
|
XM_011511731.1:c.19622A>G
(TTN)
|
XP_011510033.1:p.Tyr6541Cys
|
|
XM_017004819.1:c.45665A>G
(TTN)
|
XP_016860308.1:p.Tyr15222Cys
|
|
XM_017004820.1:c.41063A>G
(TTN)
|
XP_016860309.1:p.Tyr13688Cys
|
|
XM_017004821.1:c.41060A>G
(TTN)
|
XP_016860310.1:p.Tyr13687Cys
|
|
XM_017004822.1:c.38102A>G
(TTN)
|
XP_016860311.1:p.Tyr12701Cys
|
|
XM_017004823.1:c.19718A>G
(TTN)
|
XP_016860312.1:p.Tyr6573Cys
|
|
XM_024453094.1:c.41213A>G
(TTN)
|
XP_024308862.1:p.Tyr13738Cys
|
|
XM_024453095.1:c.41210A>G
(TTN)
|
XP_024308863.1:p.Tyr13737Cys
|
|
XM_024453096.1:c.40643A>G
(TTN)
|
XP_024308864.1:p.Tyr13548Cys
|
|
XM_024453097.1:c.37985A>G
(TTN)
|
XP_024308865.1:p.Tyr12662Cys
|
|
XM_024453098.1:c.37904A>G
(TTN)
|
XP_024308866.1:p.Tyr12635Cys
|
|
XM_024453099.1:c.19667A>G
(TTN)
|
XP_024308867.1:p.Tyr6556Cys
|
|
XM_024453100.1:c.9521A>G
(TTN)
|
XP_024308868.1:p.Tyr3174Cys
|
|