ENST00000342992.11:c.51338C>A
(TTN)
|
ENSP00000343764.6:p.Pro17113Gln
|
|
ENST00000342175.11:c.32423C>A
(TTN)
|
ENSP00000340554.6:p.Pro10808Gln
|
|
ENST00000359218.10:c.32222C>A
(TTN)
|
ENSP00000352154.5:p.Pro10741Gln
|
|
ENST00000342175.10:c.32423C>A
(TTN)
|
ENSP00000340554.6:p.Pro10808Gln
|
|
ENST00000342992.10:c.51338C>A
(TTN)
|
ENSP00000343764.6:p.Pro17113Gln
|
|
ENST00000359218.9:c.32222C>A
(TTN)
|
ENSP00000352154.5:p.Pro10741Gln
|
|
ENST00000460472.6:c.31847C>A
(TTN)
|
ENSP00000434586.1:p.Pro10616Gln
|
|
ENST00000589042.5:c.59042C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19681Gln
|
|
ENST00000591111.5:c.54119C>A
(TTN)
|
ENSP00000465570.1:p.Pro18040Gln
|
|
ENST00000615779.4:c.54119C>A
(TTN)
|
ENSP00000483597.1:p.Pro18040Gln
|
|
NM_001256850.1:c.54119C>A
(TTN)
|
NP_001243779.1:p.Pro18040Gln
|
|
NM_001267550.2:c.59042C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19681Gln
|
|
NM_003319.4:c.31847C>A
(TTN)
|
NP_003310.4:p.Pro10616Gln
|
|
NM_133378.4:c.51338C>A
(TTN)
|
NP_596869.4:p.Pro17113Gln
|
|
NM_133432.3:c.32222C>A
(TTN)
|
NP_597676.3:p.Pro10741Gln
|
|
NM_133437.4:c.32423C>A
(TTN)
|
NP_597681.4:p.Pro10808Gln
|
|
NR_038271.1:n.597-4519G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1763G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.58139C>A
(TTN)
|
XP_011510031.1:p.Pro19380Gln
|
|
XM_011511730.1:c.32033C>A
(TTN)
|
XP_011510032.1:p.Pro10678Gln
|
|
XM_011511731.1:c.31892C>A
(TTN)
|
XP_011510033.1:p.Pro10631Gln
|
|
XM_017004819.1:c.57935C>A
(TTN)
|
XP_016860308.1:p.Pro19312Gln
|
|
XM_017004820.1:c.53333C>A
(TTN)
|
XP_016860309.1:p.Pro17778Gln
|
|
XM_017004821.1:c.53330C>A
(TTN)
|
XP_016860310.1:p.Pro17777Gln
|
|
XM_017004822.1:c.50372C>A
(TTN)
|
XP_016860311.1:p.Pro16791Gln
|
|
XM_017004823.1:c.31988C>A
(TTN)
|
XP_016860312.1:p.Pro10663Gln
|
|
XM_024453094.1:c.53483C>A
(TTN)
|
XP_024308862.1:p.Pro17828Gln
|
|
XM_024453095.1:c.53480C>A
(TTN)
|
XP_024308863.1:p.Pro17827Gln
|
|
XM_024453096.1:c.52913C>A
(TTN)
|
XP_024308864.1:p.Pro17638Gln
|
|
XM_024453097.1:c.50255C>A
(TTN)
|
XP_024308865.1:p.Pro16752Gln
|
|
XM_024453098.1:c.50174C>A
(TTN)
|
XP_024308866.1:p.Pro16725Gln
|
|
XM_024453099.1:c.31937C>A
(TTN)
|
XP_024308867.1:p.Pro10646Gln
|
|
XM_024453100.1:c.21791C>A
(TTN)
|
XP_024308868.1:p.Pro7264Gln
|
|