ENST00000342992.11:c.88055A>C
(TTN)
|
ENSP00000343764.6:p.Asp29352Ala
|
|
ENST00000342175.11:c.69140A>C
(TTN)
|
ENSP00000340554.6:p.Asp23047Ala
|
|
ENST00000359218.10:c.68939A>C
(TTN)
|
ENSP00000352154.5:p.Asp22980Ala
|
|
ENST00000342175.10:c.69140A>C
(TTN)
|
ENSP00000340554.6:p.Asp23047Ala
|
|
ENST00000342992.10:c.88055A>C
(TTN)
|
ENSP00000343764.6:p.Asp29352Ala
|
|
ENST00000359218.9:c.68939A>C
(TTN)
|
ENSP00000352154.5:p.Asp22980Ala
|
|
ENST00000460472.6:c.68564A>C
(TTN)
|
ENSP00000434586.1:p.Asp22855Ala
|
|
ENST00000589042.5:c.95759A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31920Ala
|
|
ENST00000591111.5:c.90836A>C
(TTN)
|
ENSP00000465570.1:p.Asp30279Ala
|
|
ENST00000615779.4:c.90836A>C
(TTN)
|
ENSP00000483597.1:p.Asp30279Ala
|
|
NM_001256850.1:c.90836A>C
(TTN)
|
NP_001243779.1:p.Asp30279Ala
|
|
NM_001267550.2:c.95759A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31920Ala
|
|
NM_003319.4:c.68564A>C
(TTN)
|
NP_003310.4:p.Asp22855Ala
|
|
NM_133378.4:c.88055A>C
(TTN)
|
NP_596869.4:p.Asp29352Ala
|
|
NM_133432.3:c.68939A>C
(TTN)
|
NP_597676.3:p.Asp22980Ala
|
|
NM_133437.4:c.69140A>C
(TTN)
|
NP_597681.4:p.Asp23047Ala
|
|
NR_038271.1:n.446+20834T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2109T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.94856A>C
(TTN)
|
XP_011510031.1:p.Asp31619Ala
|
|
XM_011511730.1:c.68750A>C
(TTN)
|
XP_011510032.1:p.Asp22917Ala
|
|
XM_011511731.1:c.68609A>C
(TTN)
|
XP_011510033.1:p.Asp22870Ala
|
|
XM_017004819.1:c.94652A>C
(TTN)
|
XP_016860308.1:p.Asp31551Ala
|
|
XM_017004820.1:c.90050A>C
(TTN)
|
XP_016860309.1:p.Asp30017Ala
|
|
XM_017004821.1:c.90047A>C
(TTN)
|
XP_016860310.1:p.Asp30016Ala
|
|
XM_017004822.1:c.87089A>C
(TTN)
|
XP_016860311.1:p.Asp29030Ala
|
|
XM_017004823.1:c.68705A>C
(TTN)
|
XP_016860312.1:p.Asp22902Ala
|
|
XM_024453094.1:c.90200A>C
(TTN)
|
XP_024308862.1:p.Asp30067Ala
|
|
XM_024453095.1:c.90197A>C
(TTN)
|
XP_024308863.1:p.Asp30066Ala
|
|
XM_024453096.1:c.89630A>C
(TTN)
|
XP_024308864.1:p.Asp29877Ala
|
|
XM_024453097.1:c.86972A>C
(TTN)
|
XP_024308865.1:p.Asp28991Ala
|
|
XM_024453098.1:c.86891A>C
(TTN)
|
XP_024308866.1:p.Asp28964Ala
|
|
XM_024453099.1:c.68654A>C
(TTN)
|
XP_024308867.1:p.Asp22885Ala
|
|
XM_024453100.1:c.58508A>C
(TTN)
|
XP_024308868.1:p.Asp19503Ala
|
|