ENST00000342992.11:c.88174C>T
(TTN)
|
ENSP00000343764.6:p.His29392Tyr
|
|
ENST00000342175.11:c.69259C>T
(TTN)
|
ENSP00000340554.6:p.His23087Tyr
|
|
ENST00000359218.10:c.69058C>T
(TTN)
|
ENSP00000352154.5:p.His23020Tyr
|
|
ENST00000342175.10:c.69259C>T
(TTN)
|
ENSP00000340554.6:p.His23087Tyr
|
|
ENST00000342992.10:c.88174C>T
(TTN)
|
ENSP00000343764.6:p.His29392Tyr
|
|
ENST00000359218.9:c.69058C>T
(TTN)
|
ENSP00000352154.5:p.His23020Tyr
|
|
ENST00000460472.6:c.68683C>T
(TTN)
|
ENSP00000434586.1:p.His22895Tyr
|
|
ENST00000589042.5:c.95878C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.His31960Tyr
|
|
ENST00000591111.5:c.90955C>T
(TTN)
|
ENSP00000465570.1:p.His30319Tyr
|
|
ENST00000615779.4:c.90955C>T
(TTN)
|
ENSP00000483597.1:p.His30319Tyr
|
|
NM_001256850.1:c.90955C>T
(TTN)
|
NP_001243779.1:p.His30319Tyr
|
|
NM_001267550.2:c.95878C>T
(TTN)
MANE Select
|
NP_001254479.2:p.His31960Tyr
|
|
NM_003319.4:c.68683C>T
(TTN)
|
NP_003310.4:p.His22895Tyr
|
|
NM_133378.4:c.88174C>T
(TTN)
|
NP_596869.4:p.His29392Tyr
|
|
NM_133432.3:c.69058C>T
(TTN)
|
NP_597676.3:p.His23020Tyr
|
|
NM_133437.4:c.69259C>T
(TTN)
|
NP_597681.4:p.His23087Tyr
|
|
NR_038271.1:n.446+20715G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1990G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.94975C>T
(TTN)
|
XP_011510031.1:p.His31659Tyr
|
|
XM_011511730.1:c.68869C>T
(TTN)
|
XP_011510032.1:p.His22957Tyr
|
|
XM_011511731.1:c.68728C>T
(TTN)
|
XP_011510033.1:p.His22910Tyr
|
|
XM_017004819.1:c.94771C>T
(TTN)
|
XP_016860308.1:p.His31591Tyr
|
|
XM_017004820.1:c.90169C>T
(TTN)
|
XP_016860309.1:p.His30057Tyr
|
|
XM_017004821.1:c.90166C>T
(TTN)
|
XP_016860310.1:p.His30056Tyr
|
|
XM_017004822.1:c.87208C>T
(TTN)
|
XP_016860311.1:p.His29070Tyr
|
|
XM_017004823.1:c.68824C>T
(TTN)
|
XP_016860312.1:p.His22942Tyr
|
|
XM_024453094.1:c.90319C>T
(TTN)
|
XP_024308862.1:p.His30107Tyr
|
|
XM_024453095.1:c.90316C>T
(TTN)
|
XP_024308863.1:p.His30106Tyr
|
|
XM_024453096.1:c.89749C>T
(TTN)
|
XP_024308864.1:p.His29917Tyr
|
|
XM_024453097.1:c.87091C>T
(TTN)
|
XP_024308865.1:p.His29031Tyr
|
|
XM_024453098.1:c.87010C>T
(TTN)
|
XP_024308866.1:p.His29004Tyr
|
|
XM_024453099.1:c.68773C>T
(TTN)
|
XP_024308867.1:p.His22925Tyr
|
|
XM_024453100.1:c.58627C>T
(TTN)
|
XP_024308868.1:p.His19543Tyr
|
|