ENST00000342992.11:c.69422A>G
(TTN)
|
ENSP00000343764.6:p.Asp23141Gly
|
|
ENST00000342175.11:c.50507A>G
(TTN)
|
ENSP00000340554.6:p.Asp16836Gly
|
|
ENST00000359218.10:c.50306A>G
(TTN)
|
ENSP00000352154.5:p.Asp16769Gly
|
|
ENST00000342175.10:c.50507A>G
(TTN)
|
ENSP00000340554.6:p.Asp16836Gly
|
|
ENST00000342992.10:c.69422A>G
(TTN)
|
ENSP00000343764.6:p.Asp23141Gly
|
|
ENST00000359218.9:c.50306A>G
(TTN)
|
ENSP00000352154.5:p.Asp16769Gly
|
|
ENST00000460472.6:c.49931A>G
(TTN)
|
ENSP00000434586.1:p.Asp16644Gly
|
|
ENST00000589042.5:c.77126A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp25709Gly
|
|
ENST00000591111.5:c.72203A>G
(TTN)
|
ENSP00000465570.1:p.Asp24068Gly
|
|
ENST00000615779.4:c.72203A>G
(TTN)
|
ENSP00000483597.1:p.Asp24068Gly
|
|
NM_001256850.1:c.72203A>G
(TTN)
|
NP_001243779.1:p.Asp24068Gly
|
|
NM_001267550.2:c.77126A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asp25709Gly
|
|
NM_003319.4:c.49931A>G
(TTN)
|
NP_003310.4:p.Asp16644Gly
|
|
NM_133378.4:c.69422A>G
(TTN)
|
NP_596869.4:p.Asp23141Gly
|
|
NM_133432.3:c.50306A>G
(TTN)
|
NP_597676.3:p.Asp16769Gly
|
|
NM_133437.4:c.50507A>G
(TTN)
|
NP_597681.4:p.Asp16836Gly
|
|
NR_038271.1:n.447-2294T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-13566T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.76223A>G
(TTN)
|
XP_011510031.1:p.Asp25408Gly
|
|
XM_011511730.1:c.50117A>G
(TTN)
|
XP_011510032.1:p.Asp16706Gly
|
|
XM_011511731.1:c.49976A>G
(TTN)
|
XP_011510033.1:p.Asp16659Gly
|
|
XM_017004819.1:c.76019A>G
(TTN)
|
XP_016860308.1:p.Asp25340Gly
|
|
XM_017004820.1:c.71417A>G
(TTN)
|
XP_016860309.1:p.Asp23806Gly
|
|
XM_017004821.1:c.71414A>G
(TTN)
|
XP_016860310.1:p.Asp23805Gly
|
|
XM_017004822.1:c.68456A>G
(TTN)
|
XP_016860311.1:p.Asp22819Gly
|
|
XM_017004823.1:c.50072A>G
(TTN)
|
XP_016860312.1:p.Asp16691Gly
|
|
XM_024453094.1:c.71567A>G
(TTN)
|
XP_024308862.1:p.Asp23856Gly
|
|
XM_024453095.1:c.71564A>G
(TTN)
|
XP_024308863.1:p.Asp23855Gly
|
|
XM_024453096.1:c.70997A>G
(TTN)
|
XP_024308864.1:p.Asp23666Gly
|
|
XM_024453097.1:c.68339A>G
(TTN)
|
XP_024308865.1:p.Asp22780Gly
|
|
XM_024453098.1:c.68258A>G
(TTN)
|
XP_024308866.1:p.Asp22753Gly
|
|
XM_024453099.1:c.50021A>G
(TTN)
|
XP_024308867.1:p.Asp16674Gly
|
|
XM_024453100.1:c.39875A>G
(TTN)
|
XP_024308868.1:p.Asp13292Gly
|
|