ENST00000342992.11:c.53087T>C
(TTN)
|
ENSP00000343764.6:p.Val17696Ala
|
|
ENST00000342175.11:c.34172T>C
(TTN)
|
ENSP00000340554.6:p.Val11391Ala
|
|
ENST00000359218.10:c.33971T>C
(TTN)
|
ENSP00000352154.5:p.Val11324Ala
|
|
ENST00000342175.10:c.34172T>C
(TTN)
|
ENSP00000340554.6:p.Val11391Ala
|
|
ENST00000342992.10:c.53087T>C
(TTN)
|
ENSP00000343764.6:p.Val17696Ala
|
|
ENST00000359218.9:c.33971T>C
(TTN)
|
ENSP00000352154.5:p.Val11324Ala
|
|
ENST00000460472.6:c.33596T>C
(TTN)
|
ENSP00000434586.1:p.Val11199Ala
|
|
ENST00000589042.5:c.60791T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val20264Ala
|
|
ENST00000591111.5:c.55868T>C
(TTN)
|
ENSP00000465570.1:p.Val18623Ala
|
|
ENST00000615779.4:c.55868T>C
(TTN)
|
ENSP00000483597.1:p.Val18623Ala
|
|
NM_001256850.1:c.55868T>C
(TTN)
|
NP_001243779.1:p.Val18623Ala
|
|
NM_001267550.2:c.60791T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val20264Ala
|
|
NM_003319.4:c.33596T>C
(TTN)
|
NP_003310.4:p.Val11199Ala
|
|
NM_133378.4:c.53087T>C
(TTN)
|
NP_596869.4:p.Val17696Ala
|
|
NM_133432.3:c.33971T>C
(TTN)
|
NP_597676.3:p.Val11324Ala
|
|
NM_133437.4:c.34172T>C
(TTN)
|
NP_597681.4:p.Val11391Ala
|
|
NR_038271.1:n.597-6662A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-205A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.59888T>C
(TTN)
|
XP_011510031.1:p.Val19963Ala
|
|
XM_011511730.1:c.33782T>C
(TTN)
|
XP_011510032.1:p.Val11261Ala
|
|
XM_011511731.1:c.33641T>C
(TTN)
|
XP_011510033.1:p.Val11214Ala
|
|
XM_017004819.1:c.59684T>C
(TTN)
|
XP_016860308.1:p.Val19895Ala
|
|
XM_017004820.1:c.55082T>C
(TTN)
|
XP_016860309.1:p.Val18361Ala
|
|
XM_017004821.1:c.55079T>C
(TTN)
|
XP_016860310.1:p.Val18360Ala
|
|
XM_017004822.1:c.52121T>C
(TTN)
|
XP_016860311.1:p.Val17374Ala
|
|
XM_017004823.1:c.33737T>C
(TTN)
|
XP_016860312.1:p.Val11246Ala
|
|
XM_024453094.1:c.55232T>C
(TTN)
|
XP_024308862.1:p.Val18411Ala
|
|
XM_024453095.1:c.55229T>C
(TTN)
|
XP_024308863.1:p.Val18410Ala
|
|
XM_024453096.1:c.54662T>C
(TTN)
|
XP_024308864.1:p.Val18221Ala
|
|
XM_024453097.1:c.52004T>C
(TTN)
|
XP_024308865.1:p.Val17335Ala
|
|
XM_024453098.1:c.51923T>C
(TTN)
|
XP_024308866.1:p.Val17308Ala
|
|
XM_024453099.1:c.33686T>C
(TTN)
|
XP_024308867.1:p.Val11229Ala
|
|
XM_024453100.1:c.23540T>C
(TTN)
|
XP_024308868.1:p.Val7847Ala
|
|