|
NM_001267550.2:c.92682C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Phe30894=
|
|
ENST00000589042.5:c.92682C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Phe30894=
|
|
NM_001256850.1:c.87759C>T
(TTN)
|
NP_001243779.1:p.Phe29253=
|
|
NM_003319.4:c.65487C>T
(TTN)
|
NP_003310.4:p.Phe21829=
|
|
NM_133378.4:c.84978C>T
(TTN)
|
NP_596869.4:p.Phe28326=
|
|
NM_133432.3:c.65862C>T
(TTN)
|
NP_597676.3:p.Phe21954=
|
|
NM_133437.4:c.66063C>T
(TTN)
|
NP_597681.4:p.Phe22021=
|
|
NR_038271.1:n.447-22356G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6583G>A
(TTN-AS1)
|
|
|
ENST00000342175.10:c.66063C>T
(TTN)
|
ENSP00000340554.6:p.Phe22021=
|
|
ENST00000342175.11:c.66063C>T
(TTN)
|
ENSP00000340554.6:p.Phe22021=
|
|
ENST00000342992.10:c.84978C>T
(TTN)
|
ENSP00000343764.6:p.Phe28326=
|
|
ENST00000342992.11:c.84978C>T
(TTN)
|
ENSP00000343764.6:p.Phe28326=
|
|
ENST00000359218.10:c.65862C>T
(TTN)
|
ENSP00000352154.5:p.Phe21954=
|
|
ENST00000359218.9:c.65862C>T
(TTN)
|
ENSP00000352154.5:p.Phe21954=
|
|
ENST00000460472.6:c.65487C>T
(TTN)
|
ENSP00000434586.1:p.Phe21829=
|
|
ENST00000591111.5:c.87759C>T
(TTN)
|
ENSP00000465570.1:p.Phe29253=
|
|
ENST00000615779.4:c.87759C>T
(TTN)
|
ENSP00000483597.1:p.Phe29253=
|
|
XM_011511729.1:c.91779C>T
(TTN)
|
XP_011510031.1:p.Phe30593=
|
|
XM_011511730.1:c.65673C>T
(TTN)
|
XP_011510032.1:p.Phe21891=
|
|
XM_011511731.1:c.65532C>T
(TTN)
|
XP_011510033.1:p.Phe21844=
|
|
XM_017004819.1:c.91575C>T
(TTN)
|
XP_016860308.1:p.Phe30525=
|
|
XM_017004820.1:c.86973C>T
(TTN)
|
XP_016860309.1:p.Phe28991=
|
|
XM_017004821.1:c.86970C>T
(TTN)
|
XP_016860310.1:p.Phe28990=
|
|
XM_017004822.1:c.84012C>T
(TTN)
|
XP_016860311.1:p.Phe28004=
|
|
XM_017004823.1:c.65628C>T
(TTN)
|
XP_016860312.1:p.Phe21876=
|
|
XM_024453094.1:c.87123C>T
(TTN)
|
XP_024308862.1:p.Phe29041=
|
|
XM_024453095.1:c.87120C>T
(TTN)
|
XP_024308863.1:p.Phe29040=
|
|
XM_024453096.1:c.86553C>T
(TTN)
|
XP_024308864.1:p.Phe28851=
|
|
XM_024453097.1:c.83895C>T
(TTN)
|
XP_024308865.1:p.Phe27965=
|
|
XM_024453098.1:c.83814C>T
(TTN)
|
XP_024308866.1:p.Phe27938=
|
|
XM_024453099.1:c.65577C>T
(TTN)
|
XP_024308867.1:p.Phe21859=
|
|
XM_024453100.1:c.55431C>T
(TTN)
|
XP_024308868.1:p.Phe18477=
|
