ENST00000342992.11:c.76112T>C
(TTN)
|
ENSP00000343764.6:p.Val25371Ala
|
|
ENST00000342175.11:c.57197T>C
(TTN)
|
ENSP00000340554.6:p.Val19066Ala
|
|
ENST00000359218.10:c.56996T>C
(TTN)
|
ENSP00000352154.5:p.Val18999Ala
|
|
ENST00000342175.10:c.57197T>C
(TTN)
|
ENSP00000340554.6:p.Val19066Ala
|
|
ENST00000342992.10:c.76112T>C
(TTN)
|
ENSP00000343764.6:p.Val25371Ala
|
|
ENST00000359218.9:c.56996T>C
(TTN)
|
ENSP00000352154.5:p.Val18999Ala
|
|
ENST00000460472.6:c.56621T>C
(TTN)
|
ENSP00000434586.1:p.Val18874Ala
|
|
ENST00000589042.5:c.83816T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val27939Ala
|
|
ENST00000591111.5:c.78893T>C
(TTN)
|
ENSP00000465570.1:p.Val26298Ala
|
|
ENST00000615779.4:c.78893T>C
(TTN)
|
ENSP00000483597.1:p.Val26298Ala
|
|
NM_001256850.1:c.78893T>C
(TTN)
|
NP_001243779.1:p.Val26298Ala
|
|
NM_001267550.2:c.83816T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Val27939Ala
|
|
NM_003319.4:c.56621T>C
(TTN)
|
NP_003310.4:p.Val18874Ala
|
|
NM_133378.4:c.76112T>C
(TTN)
|
NP_596869.4:p.Val25371Ala
|
|
NM_133432.3:c.56996T>C
(TTN)
|
NP_597676.3:p.Val18999Ala
|
|
NM_133437.4:c.57197T>C
(TTN)
|
NP_597681.4:p.Val19066Ala
|
|
NR_038271.1:n.447-8984A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+19955A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.82913T>C
(TTN)
|
XP_011510031.1:p.Val27638Ala
|
|
XM_011511730.1:c.56807T>C
(TTN)
|
XP_011510032.1:p.Val18936Ala
|
|
XM_011511731.1:c.56666T>C
(TTN)
|
XP_011510033.1:p.Val18889Ala
|
|
XM_017004819.1:c.82709T>C
(TTN)
|
XP_016860308.1:p.Val27570Ala
|
|
XM_017004820.1:c.78107T>C
(TTN)
|
XP_016860309.1:p.Val26036Ala
|
|
XM_017004821.1:c.78104T>C
(TTN)
|
XP_016860310.1:p.Val26035Ala
|
|
XM_017004822.1:c.75146T>C
(TTN)
|
XP_016860311.1:p.Val25049Ala
|
|
XM_017004823.1:c.56762T>C
(TTN)
|
XP_016860312.1:p.Val18921Ala
|
|
XM_024453094.1:c.78257T>C
(TTN)
|
XP_024308862.1:p.Val26086Ala
|
|
XM_024453095.1:c.78254T>C
(TTN)
|
XP_024308863.1:p.Val26085Ala
|
|
XM_024453096.1:c.77687T>C
(TTN)
|
XP_024308864.1:p.Val25896Ala
|
|
XM_024453097.1:c.75029T>C
(TTN)
|
XP_024308865.1:p.Val25010Ala
|
|
XM_024453098.1:c.74948T>C
(TTN)
|
XP_024308866.1:p.Val24983Ala
|
|
XM_024453099.1:c.56711T>C
(TTN)
|
XP_024308867.1:p.Val18904Ala
|
|
XM_024453100.1:c.46565T>C
(TTN)
|
XP_024308868.1:p.Val15522Ala
|
|