ENST00000342992.11:c.96798T>C
(TTN)
|
ENSP00000343764.6:p.Ser32266=
|
|
ENST00000342175.11:c.77883T>C
(TTN)
|
ENSP00000340554.6:p.Ser25961=
|
|
ENST00000359218.10:c.77682T>C
(TTN)
|
ENSP00000352154.5:p.Ser25894=
|
|
ENST00000342175.10:c.77883T>C
(TTN)
|
ENSP00000340554.6:p.Ser25961=
|
|
ENST00000342992.10:c.96798T>C
(TTN)
|
ENSP00000343764.6:p.Ser32266=
|
|
ENST00000359218.9:c.77682T>C
(TTN)
|
ENSP00000352154.5:p.Ser25894=
|
|
ENST00000460472.6:c.77307T>C
(TTN)
|
ENSP00000434586.1:p.Ser25769=
|
|
ENST00000589042.5:c.104502T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34834=
|
|
ENST00000591111.5:c.99579T>C
(TTN)
|
ENSP00000465570.1:p.Ser33193=
|
|
ENST00000615779.4:c.99579T>C
(TTN)
|
ENSP00000483597.1:p.Ser33193=
|
|
NM_001256850.1:c.99579T>C
(TTN)
|
NP_001243779.1:p.Ser33193=
|
|
NM_001267550.2:c.104502T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34834=
|
|
NM_003319.4:c.77307T>C
(TTN)
|
NP_003310.4:p.Ser25769=
|
|
NM_133378.4:c.96798T>C
(TTN)
|
NP_596869.4:p.Ser32266=
|
|
NM_133432.3:c.77682T>C
(TTN)
|
NP_597676.3:p.Ser25894=
|
|
NM_133437.4:c.77883T>C
(TTN)
|
NP_597681.4:p.Ser25961=
|
|
NR_038271.1:n.446+8477A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3619A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103599T>C
(TTN)
|
XP_011510031.1:p.Ser34533=
|
|
XM_011511730.1:c.77493T>C
(TTN)
|
XP_011510032.1:p.Ser25831=
|
|
XM_011511731.1:c.77352T>C
(TTN)
|
XP_011510033.1:p.Ser25784=
|
|
XM_017004819.1:c.103395T>C
(TTN)
|
XP_016860308.1:p.Ser34465=
|
|
XM_017004820.1:c.98793T>C
(TTN)
|
XP_016860309.1:p.Ser32931=
|
|
XM_017004821.1:c.98790T>C
(TTN)
|
XP_016860310.1:p.Ser32930=
|
|
XM_017004822.1:c.95832T>C
(TTN)
|
XP_016860311.1:p.Ser31944=
|
|
XM_017004823.1:c.77448T>C
(TTN)
|
XP_016860312.1:p.Ser25816=
|
|
XM_024453094.1:c.98943T>C
(TTN)
|
XP_024308862.1:p.Ser32981=
|
|
XM_024453095.1:c.98940T>C
(TTN)
|
XP_024308863.1:p.Ser32980=
|
|
XM_024453096.1:c.98373T>C
(TTN)
|
XP_024308864.1:p.Ser32791=
|
|
XM_024453097.1:c.95715T>C
(TTN)
|
XP_024308865.1:p.Ser31905=
|
|
XM_024453098.1:c.95634T>C
(TTN)
|
XP_024308866.1:p.Ser31878=
|
|
XM_024453099.1:c.77397T>C
(TTN)
|
XP_024308867.1:p.Ser25799=
|
|
XM_024453100.1:c.67251T>C
(TTN)
|
XP_024308868.1:p.Ser22417=
|
|