ENST00000342992.11:c.96641A>G
(TTN)
|
ENSP00000343764.6:p.His32214Arg
|
|
ENST00000342175.11:c.77726A>G
(TTN)
|
ENSP00000340554.6:p.His25909Arg
|
|
ENST00000359218.10:c.77525A>G
(TTN)
|
ENSP00000352154.5:p.His25842Arg
|
|
ENST00000342175.10:c.77726A>G
(TTN)
|
ENSP00000340554.6:p.His25909Arg
|
|
ENST00000342992.10:c.96641A>G
(TTN)
|
ENSP00000343764.6:p.His32214Arg
|
|
ENST00000359218.9:c.77525A>G
(TTN)
|
ENSP00000352154.5:p.His25842Arg
|
|
ENST00000460472.6:c.77150A>G
(TTN)
|
ENSP00000434586.1:p.His25717Arg
|
|
ENST00000589042.5:c.104345A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.His34782Arg
|
|
ENST00000591111.5:c.99422A>G
(TTN)
|
ENSP00000465570.1:p.His33141Arg
|
|
ENST00000615779.4:c.99422A>G
(TTN)
|
ENSP00000483597.1:p.His33141Arg
|
|
NM_001256850.1:c.99422A>G
(TTN)
|
NP_001243779.1:p.His33141Arg
|
|
NM_001267550.2:c.104345A>G
(TTN)
MANE Select
|
NP_001254479.2:p.His34782Arg
|
|
NM_003319.4:c.77150A>G
(TTN)
|
NP_003310.4:p.His25717Arg
|
|
NM_133378.4:c.96641A>G
(TTN)
|
NP_596869.4:p.His32214Arg
|
|
NM_133432.3:c.77525A>G
(TTN)
|
NP_597676.3:p.His25842Arg
|
|
NM_133437.4:c.77726A>G
(TTN)
|
NP_597681.4:p.His25909Arg
|
|
NR_038271.1:n.446+8634T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3462T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103442A>G
(TTN)
|
XP_011510031.1:p.His34481Arg
|
|
XM_011511730.1:c.77336A>G
(TTN)
|
XP_011510032.1:p.His25779Arg
|
|
XM_011511731.1:c.77195A>G
(TTN)
|
XP_011510033.1:p.His25732Arg
|
|
XM_017004819.1:c.103238A>G
(TTN)
|
XP_016860308.1:p.His34413Arg
|
|
XM_017004820.1:c.98636A>G
(TTN)
|
XP_016860309.1:p.His32879Arg
|
|
XM_017004821.1:c.98633A>G
(TTN)
|
XP_016860310.1:p.His32878Arg
|
|
XM_017004822.1:c.95675A>G
(TTN)
|
XP_016860311.1:p.His31892Arg
|
|
XM_017004823.1:c.77291A>G
(TTN)
|
XP_016860312.1:p.His25764Arg
|
|
XM_024453094.1:c.98786A>G
(TTN)
|
XP_024308862.1:p.His32929Arg
|
|
XM_024453095.1:c.98783A>G
(TTN)
|
XP_024308863.1:p.His32928Arg
|
|
XM_024453096.1:c.98216A>G
(TTN)
|
XP_024308864.1:p.His32739Arg
|
|
XM_024453097.1:c.95558A>G
(TTN)
|
XP_024308865.1:p.His31853Arg
|
|
XM_024453098.1:c.95477A>G
(TTN)
|
XP_024308866.1:p.His31826Arg
|
|
XM_024453099.1:c.77240A>G
(TTN)
|
XP_024308867.1:p.His25747Arg
|
|
XM_024453100.1:c.67094A>G
(TTN)
|
XP_024308868.1:p.His22365Arg
|
|