ENST00000342992.11:c.88151A>C
(TTN)
|
ENSP00000343764.6:p.Asp29384Ala
|
|
ENST00000342175.11:c.69236A>C
(TTN)
|
ENSP00000340554.6:p.Asp23079Ala
|
|
ENST00000359218.10:c.69035A>C
(TTN)
|
ENSP00000352154.5:p.Asp23012Ala
|
|
ENST00000342175.10:c.69236A>C
(TTN)
|
ENSP00000340554.6:p.Asp23079Ala
|
|
ENST00000342992.10:c.88151A>C
(TTN)
|
ENSP00000343764.6:p.Asp29384Ala
|
|
ENST00000359218.9:c.69035A>C
(TTN)
|
ENSP00000352154.5:p.Asp23012Ala
|
|
ENST00000460472.6:c.68660A>C
(TTN)
|
ENSP00000434586.1:p.Asp22887Ala
|
|
ENST00000589042.5:c.95855A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31952Ala
|
|
ENST00000591111.5:c.90932A>C
(TTN)
|
ENSP00000465570.1:p.Asp30311Ala
|
|
ENST00000615779.4:c.90932A>C
(TTN)
|
ENSP00000483597.1:p.Asp30311Ala
|
|
NM_001256850.1:c.90932A>C
(TTN)
|
NP_001243779.1:p.Asp30311Ala
|
|
NM_001267550.2:c.95855A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31952Ala
|
|
NM_003319.4:c.68660A>C
(TTN)
|
NP_003310.4:p.Asp22887Ala
|
|
NM_133378.4:c.88151A>C
(TTN)
|
NP_596869.4:p.Asp29384Ala
|
|
NM_133432.3:c.69035A>C
(TTN)
|
NP_597676.3:p.Asp23012Ala
|
|
NM_133437.4:c.69236A>C
(TTN)
|
NP_597681.4:p.Asp23079Ala
|
|
NR_038271.1:n.446+20738T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2013T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.94952A>C
(TTN)
|
XP_011510031.1:p.Asp31651Ala
|
|
XM_011511730.1:c.68846A>C
(TTN)
|
XP_011510032.1:p.Asp22949Ala
|
|
XM_011511731.1:c.68705A>C
(TTN)
|
XP_011510033.1:p.Asp22902Ala
|
|
XM_017004819.1:c.94748A>C
(TTN)
|
XP_016860308.1:p.Asp31583Ala
|
|
XM_017004820.1:c.90146A>C
(TTN)
|
XP_016860309.1:p.Asp30049Ala
|
|
XM_017004821.1:c.90143A>C
(TTN)
|
XP_016860310.1:p.Asp30048Ala
|
|
XM_017004822.1:c.87185A>C
(TTN)
|
XP_016860311.1:p.Asp29062Ala
|
|
XM_017004823.1:c.68801A>C
(TTN)
|
XP_016860312.1:p.Asp22934Ala
|
|
XM_024453094.1:c.90296A>C
(TTN)
|
XP_024308862.1:p.Asp30099Ala
|
|
XM_024453095.1:c.90293A>C
(TTN)
|
XP_024308863.1:p.Asp30098Ala
|
|
XM_024453096.1:c.89726A>C
(TTN)
|
XP_024308864.1:p.Asp29909Ala
|
|
XM_024453097.1:c.87068A>C
(TTN)
|
XP_024308865.1:p.Asp29023Ala
|
|
XM_024453098.1:c.86987A>C
(TTN)
|
XP_024308866.1:p.Asp28996Ala
|
|
XM_024453099.1:c.68750A>C
(TTN)
|
XP_024308867.1:p.Asp22917Ala
|
|
XM_024453100.1:c.58604A>C
(TTN)
|
XP_024308868.1:p.Asp19535Ala
|
|