ENST00000342992.11:c.98299C>T
(TTN)
|
ENSP00000343764.6:p.His32767Tyr
|
|
ENST00000342175.11:c.79384C>T
(TTN)
|
ENSP00000340554.6:p.His26462Tyr
|
|
ENST00000359218.10:c.79183C>T
(TTN)
|
ENSP00000352154.5:p.His26395Tyr
|
|
ENST00000342175.10:c.79384C>T
(TTN)
|
ENSP00000340554.6:p.His26462Tyr
|
|
ENST00000342992.10:c.98299C>T
(TTN)
|
ENSP00000343764.6:p.His32767Tyr
|
|
ENST00000359218.9:c.79183C>T
(TTN)
|
ENSP00000352154.5:p.His26395Tyr
|
|
ENST00000460472.6:c.78808C>T
(TTN)
|
ENSP00000434586.1:p.His26270Tyr
|
|
ENST00000589042.5:c.106003C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.His35335Tyr
|
|
ENST00000591111.5:c.101080C>T
(TTN)
|
ENSP00000465570.1:p.His33694Tyr
|
|
ENST00000615779.4:c.101080C>T
(TTN)
|
ENSP00000483597.1:p.His33694Tyr
|
|
NM_001256850.1:c.101080C>T
(TTN)
|
NP_001243779.1:p.His33694Tyr
|
|
NM_001267550.2:c.106003C>T
(TTN)
MANE Select
|
NP_001254479.2:p.His35335Tyr
|
|
NM_003319.4:c.78808C>T
(TTN)
|
NP_003310.4:p.His26270Tyr
|
|
NM_133378.4:c.98299C>T
(TTN)
|
NP_596869.4:p.His32767Tyr
|
|
NM_133432.3:c.79183C>T
(TTN)
|
NP_597676.3:p.His26395Tyr
|
|
NM_133437.4:c.79384C>T
(TTN)
|
NP_597681.4:p.His26462Tyr
|
|
NR_038271.1:n.446+6976G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5120G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.105100C>T
(TTN)
|
XP_011510031.1:p.His35034Tyr
|
|
XM_011511730.1:c.78994C>T
(TTN)
|
XP_011510032.1:p.His26332Tyr
|
|
XM_011511731.1:c.78853C>T
(TTN)
|
XP_011510033.1:p.His26285Tyr
|
|
XM_017004819.1:c.104896C>T
(TTN)
|
XP_016860308.1:p.His34966Tyr
|
|
XM_017004820.1:c.100294C>T
(TTN)
|
XP_016860309.1:p.His33432Tyr
|
|
XM_017004821.1:c.100291C>T
(TTN)
|
XP_016860310.1:p.His33431Tyr
|
|
XM_017004822.1:c.97333C>T
(TTN)
|
XP_016860311.1:p.His32445Tyr
|
|
XM_017004823.1:c.78949C>T
(TTN)
|
XP_016860312.1:p.His26317Tyr
|
|
XM_024453094.1:c.100444C>T
(TTN)
|
XP_024308862.1:p.His33482Tyr
|
|
XM_024453095.1:c.100441C>T
(TTN)
|
XP_024308863.1:p.His33481Tyr
|
|
XM_024453096.1:c.99874C>T
(TTN)
|
XP_024308864.1:p.His33292Tyr
|
|
XM_024453097.1:c.97216C>T
(TTN)
|
XP_024308865.1:p.His32406Tyr
|
|
XM_024453098.1:c.97135C>T
(TTN)
|
XP_024308866.1:p.His32379Tyr
|
|
XM_024453099.1:c.78898C>T
(TTN)
|
XP_024308867.1:p.His26300Tyr
|
|
XM_024453100.1:c.68752C>T
(TTN)
|
XP_024308868.1:p.His22918Tyr
|
|