ENST00000342992.11:c.51364A>G
(TTN)
|
ENSP00000343764.6:p.Ile17122Val
|
|
ENST00000342175.11:c.32449A>G
(TTN)
|
ENSP00000340554.6:p.Ile10817Val
|
|
ENST00000359218.10:c.32248A>G
(TTN)
|
ENSP00000352154.5:p.Ile10750Val
|
|
ENST00000342175.10:c.32449A>G
(TTN)
|
ENSP00000340554.6:p.Ile10817Val
|
|
ENST00000342992.10:c.51364A>G
(TTN)
|
ENSP00000343764.6:p.Ile17122Val
|
|
ENST00000359218.9:c.32248A>G
(TTN)
|
ENSP00000352154.5:p.Ile10750Val
|
|
ENST00000460472.6:c.31873A>G
(TTN)
|
ENSP00000434586.1:p.Ile10625Val
|
|
ENST00000589042.5:c.59068A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile19690Val
|
|
ENST00000591111.5:c.54145A>G
(TTN)
|
ENSP00000465570.1:p.Ile18049Val
|
|
ENST00000615779.4:c.54145A>G
(TTN)
|
ENSP00000483597.1:p.Ile18049Val
|
|
NM_001256850.1:c.54145A>G
(TTN)
|
NP_001243779.1:p.Ile18049Val
|
|
NM_001267550.2:c.59068A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ile19690Val
|
|
NM_003319.4:c.31873A>G
(TTN)
|
NP_003310.4:p.Ile10625Val
|
|
NM_133378.4:c.51364A>G
(TTN)
|
NP_596869.4:p.Ile17122Val
|
|
NM_133432.3:c.32248A>G
(TTN)
|
NP_597676.3:p.Ile10750Val
|
|
NM_133437.4:c.32449A>G
(TTN)
|
NP_597681.4:p.Ile10817Val
|
|
NR_038271.1:n.597-4545T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1737T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.58165A>G
(TTN)
|
XP_011510031.1:p.Ile19389Val
|
|
XM_011511730.1:c.32059A>G
(TTN)
|
XP_011510032.1:p.Ile10687Val
|
|
XM_011511731.1:c.31918A>G
(TTN)
|
XP_011510033.1:p.Ile10640Val
|
|
XM_017004819.1:c.57961A>G
(TTN)
|
XP_016860308.1:p.Ile19321Val
|
|
XM_017004820.1:c.53359A>G
(TTN)
|
XP_016860309.1:p.Ile17787Val
|
|
XM_017004821.1:c.53356A>G
(TTN)
|
XP_016860310.1:p.Ile17786Val
|
|
XM_017004822.1:c.50398A>G
(TTN)
|
XP_016860311.1:p.Ile16800Val
|
|
XM_017004823.1:c.32014A>G
(TTN)
|
XP_016860312.1:p.Ile10672Val
|
|
XM_024453094.1:c.53509A>G
(TTN)
|
XP_024308862.1:p.Ile17837Val
|
|
XM_024453095.1:c.53506A>G
(TTN)
|
XP_024308863.1:p.Ile17836Val
|
|
XM_024453096.1:c.52939A>G
(TTN)
|
XP_024308864.1:p.Ile17647Val
|
|
XM_024453097.1:c.50281A>G
(TTN)
|
XP_024308865.1:p.Ile16761Val
|
|
XM_024453098.1:c.50200A>G
(TTN)
|
XP_024308866.1:p.Ile16734Val
|
|
XM_024453099.1:c.31963A>G
(TTN)
|
XP_024308867.1:p.Ile10655Val
|
|
XM_024453100.1:c.21817A>G
(TTN)
|
XP_024308868.1:p.Ile7273Val
|
|