ENST00000342992.11:c.96640C>T
(TTN)
|
ENSP00000343764.6:p.His32214Tyr
|
|
ENST00000342175.11:c.77725C>T
(TTN)
|
ENSP00000340554.6:p.His25909Tyr
|
|
ENST00000359218.10:c.77524C>T
(TTN)
|
ENSP00000352154.5:p.His25842Tyr
|
|
ENST00000342175.10:c.77725C>T
(TTN)
|
ENSP00000340554.6:p.His25909Tyr
|
|
ENST00000342992.10:c.96640C>T
(TTN)
|
ENSP00000343764.6:p.His32214Tyr
|
|
ENST00000359218.9:c.77524C>T
(TTN)
|
ENSP00000352154.5:p.His25842Tyr
|
|
ENST00000460472.6:c.77149C>T
(TTN)
|
ENSP00000434586.1:p.His25717Tyr
|
|
ENST00000589042.5:c.104344C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.His34782Tyr
|
|
ENST00000591111.5:c.99421C>T
(TTN)
|
ENSP00000465570.1:p.His33141Tyr
|
|
ENST00000615779.4:c.99421C>T
(TTN)
|
ENSP00000483597.1:p.His33141Tyr
|
|
NM_001256850.1:c.99421C>T
(TTN)
|
NP_001243779.1:p.His33141Tyr
|
|
NM_001267550.2:c.104344C>T
(TTN)
MANE Select
|
NP_001254479.2:p.His34782Tyr
|
|
NM_003319.4:c.77149C>T
(TTN)
|
NP_003310.4:p.His25717Tyr
|
|
NM_133378.4:c.96640C>T
(TTN)
|
NP_596869.4:p.His32214Tyr
|
|
NM_133432.3:c.77524C>T
(TTN)
|
NP_597676.3:p.His25842Tyr
|
|
NM_133437.4:c.77725C>T
(TTN)
|
NP_597681.4:p.His25909Tyr
|
|
NR_038271.1:n.446+8635G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3461G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.103441C>T
(TTN)
|
XP_011510031.1:p.His34481Tyr
|
|
XM_011511730.1:c.77335C>T
(TTN)
|
XP_011510032.1:p.His25779Tyr
|
|
XM_011511731.1:c.77194C>T
(TTN)
|
XP_011510033.1:p.His25732Tyr
|
|
XM_017004819.1:c.103237C>T
(TTN)
|
XP_016860308.1:p.His34413Tyr
|
|
XM_017004820.1:c.98635C>T
(TTN)
|
XP_016860309.1:p.His32879Tyr
|
|
XM_017004821.1:c.98632C>T
(TTN)
|
XP_016860310.1:p.His32878Tyr
|
|
XM_017004822.1:c.95674C>T
(TTN)
|
XP_016860311.1:p.His31892Tyr
|
|
XM_017004823.1:c.77290C>T
(TTN)
|
XP_016860312.1:p.His25764Tyr
|
|
XM_024453094.1:c.98785C>T
(TTN)
|
XP_024308862.1:p.His32929Tyr
|
|
XM_024453095.1:c.98782C>T
(TTN)
|
XP_024308863.1:p.His32928Tyr
|
|
XM_024453096.1:c.98215C>T
(TTN)
|
XP_024308864.1:p.His32739Tyr
|
|
XM_024453097.1:c.95557C>T
(TTN)
|
XP_024308865.1:p.His31853Tyr
|
|
XM_024453098.1:c.95476C>T
(TTN)
|
XP_024308866.1:p.His31826Tyr
|
|
XM_024453099.1:c.77239C>T
(TTN)
|
XP_024308867.1:p.His25747Tyr
|
|
XM_024453100.1:c.67093C>T
(TTN)
|
XP_024308868.1:p.His22365Tyr
|
|