ENST00000342992.11:c.98297T>G
(TTN)
|
ENSP00000343764.6:p.Phe32766Cys
|
|
ENST00000342175.11:c.79382T>G
(TTN)
|
ENSP00000340554.6:p.Phe26461Cys
|
|
ENST00000359218.10:c.79181T>G
(TTN)
|
ENSP00000352154.5:p.Phe26394Cys
|
|
ENST00000342175.10:c.79382T>G
(TTN)
|
ENSP00000340554.6:p.Phe26461Cys
|
|
ENST00000342992.10:c.98297T>G
(TTN)
|
ENSP00000343764.6:p.Phe32766Cys
|
|
ENST00000359218.9:c.79181T>G
(TTN)
|
ENSP00000352154.5:p.Phe26394Cys
|
|
ENST00000460472.6:c.78806T>G
(TTN)
|
ENSP00000434586.1:p.Phe26269Cys
|
|
ENST00000589042.5:c.106001T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe35334Cys
|
|
ENST00000591111.5:c.101078T>G
(TTN)
|
ENSP00000465570.1:p.Phe33693Cys
|
|
ENST00000615779.4:c.101078T>G
(TTN)
|
ENSP00000483597.1:p.Phe33693Cys
|
|
NM_001256850.1:c.101078T>G
(TTN)
|
NP_001243779.1:p.Phe33693Cys
|
|
NM_001267550.2:c.106001T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Phe35334Cys
|
|
NM_003319.4:c.78806T>G
(TTN)
|
NP_003310.4:p.Phe26269Cys
|
|
NM_133378.4:c.98297T>G
(TTN)
|
NP_596869.4:p.Phe32766Cys
|
|
NM_133432.3:c.79181T>G
(TTN)
|
NP_597676.3:p.Phe26394Cys
|
|
NM_133437.4:c.79382T>G
(TTN)
|
NP_597681.4:p.Phe26461Cys
|
|
NR_038271.1:n.446+6978A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5118A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.105098T>G
(TTN)
|
XP_011510031.1:p.Phe35033Cys
|
|
XM_011511730.1:c.78992T>G
(TTN)
|
XP_011510032.1:p.Phe26331Cys
|
|
XM_011511731.1:c.78851T>G
(TTN)
|
XP_011510033.1:p.Phe26284Cys
|
|
XM_017004819.1:c.104894T>G
(TTN)
|
XP_016860308.1:p.Phe34965Cys
|
|
XM_017004820.1:c.100292T>G
(TTN)
|
XP_016860309.1:p.Phe33431Cys
|
|
XM_017004821.1:c.100289T>G
(TTN)
|
XP_016860310.1:p.Phe33430Cys
|
|
XM_017004822.1:c.97331T>G
(TTN)
|
XP_016860311.1:p.Phe32444Cys
|
|
XM_017004823.1:c.78947T>G
(TTN)
|
XP_016860312.1:p.Phe26316Cys
|
|
XM_024453094.1:c.100442T>G
(TTN)
|
XP_024308862.1:p.Phe33481Cys
|
|
XM_024453095.1:c.100439T>G
(TTN)
|
XP_024308863.1:p.Phe33480Cys
|
|
XM_024453096.1:c.99872T>G
(TTN)
|
XP_024308864.1:p.Phe33291Cys
|
|
XM_024453097.1:c.97214T>G
(TTN)
|
XP_024308865.1:p.Phe32405Cys
|
|
XM_024453098.1:c.97133T>G
(TTN)
|
XP_024308866.1:p.Phe32378Cys
|
|
XM_024453099.1:c.78896T>G
(TTN)
|
XP_024308867.1:p.Phe26299Cys
|
|
XM_024453100.1:c.68750T>G
(TTN)
|
XP_024308868.1:p.Phe22917Cys
|
|