ENST00000342992.11:c.67880T>G
(TTN)
|
ENSP00000343764.6:p.Val22627Gly
|
|
ENST00000342175.11:c.48965T>G
(TTN)
|
ENSP00000340554.6:p.Val16322Gly
|
|
ENST00000359218.10:c.48764T>G
(TTN)
|
ENSP00000352154.5:p.Val16255Gly
|
|
ENST00000342175.10:c.48965T>G
(TTN)
|
ENSP00000340554.6:p.Val16322Gly
|
|
ENST00000342992.10:c.67880T>G
(TTN)
|
ENSP00000343764.6:p.Val22627Gly
|
|
ENST00000359218.9:c.48764T>G
(TTN)
|
ENSP00000352154.5:p.Val16255Gly
|
|
ENST00000460472.6:c.48389T>G
(TTN)
|
ENSP00000434586.1:p.Val16130Gly
|
|
ENST00000589042.5:c.75584T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val25195Gly
|
|
ENST00000591111.5:c.70661T>G
(TTN)
|
ENSP00000465570.1:p.Val23554Gly
|
|
ENST00000615779.4:c.70661T>G
(TTN)
|
ENSP00000483597.1:p.Val23554Gly
|
|
NM_001256850.1:c.70661T>G
(TTN)
|
NP_001243779.1:p.Val23554Gly
|
|
NM_001267550.2:c.75584T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val25195Gly
|
|
NM_003319.4:c.48389T>G
(TTN)
|
NP_003310.4:p.Val16130Gly
|
|
NM_133378.4:c.67880T>G
(TTN)
|
NP_596869.4:p.Val22627Gly
|
|
NM_133432.3:c.48764T>G
(TTN)
|
NP_597676.3:p.Val16255Gly
|
|
NM_133437.4:c.48965T>G
(TTN)
|
NP_597681.4:p.Val16322Gly
|
|
NR_038271.1:n.447-752A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12024A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.74681T>G
(TTN)
|
XP_011510031.1:p.Val24894Gly
|
|
XM_011511730.1:c.48575T>G
(TTN)
|
XP_011510032.1:p.Val16192Gly
|
|
XM_011511731.1:c.48434T>G
(TTN)
|
XP_011510033.1:p.Val16145Gly
|
|
XM_017004819.1:c.74477T>G
(TTN)
|
XP_016860308.1:p.Val24826Gly
|
|
XM_017004820.1:c.69875T>G
(TTN)
|
XP_016860309.1:p.Val23292Gly
|
|
XM_017004821.1:c.69872T>G
(TTN)
|
XP_016860310.1:p.Val23291Gly
|
|
XM_017004822.1:c.66914T>G
(TTN)
|
XP_016860311.1:p.Val22305Gly
|
|
XM_017004823.1:c.48530T>G
(TTN)
|
XP_016860312.1:p.Val16177Gly
|
|
XM_024453094.1:c.70025T>G
(TTN)
|
XP_024308862.1:p.Val23342Gly
|
|
XM_024453095.1:c.70022T>G
(TTN)
|
XP_024308863.1:p.Val23341Gly
|
|
XM_024453096.1:c.69455T>G
(TTN)
|
XP_024308864.1:p.Val23152Gly
|
|
XM_024453097.1:c.66797T>G
(TTN)
|
XP_024308865.1:p.Val22266Gly
|
|
XM_024453098.1:c.66716T>G
(TTN)
|
XP_024308866.1:p.Val22239Gly
|
|
XM_024453099.1:c.48479T>G
(TTN)
|
XP_024308867.1:p.Val16160Gly
|
|
XM_024453100.1:c.38333T>G
(TTN)
|
XP_024308868.1:p.Val12778Gly
|
|