ENST00000342992.11:c.94956T>A
(TTN)
|
ENSP00000343764.6:p.Ser31652=
|
|
ENST00000342175.11:c.76041T>A
(TTN)
|
ENSP00000340554.6:p.Ser25347=
|
|
ENST00000359218.10:c.75840T>A
(TTN)
|
ENSP00000352154.5:p.Ser25280=
|
|
ENST00000342175.10:c.76041T>A
(TTN)
|
ENSP00000340554.6:p.Ser25347=
|
|
ENST00000342992.10:c.94956T>A
(TTN)
|
ENSP00000343764.6:p.Ser31652=
|
|
ENST00000359218.9:c.75840T>A
(TTN)
|
ENSP00000352154.5:p.Ser25280=
|
|
ENST00000460472.6:c.75465T>A
(TTN)
|
ENSP00000434586.1:p.Ser25155=
|
|
ENST00000589042.5:c.102660T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34220=
|
|
ENST00000591111.5:c.97737T>A
(TTN)
|
ENSP00000465570.1:p.Ser32579=
|
|
ENST00000615779.4:c.97737T>A
(TTN)
|
ENSP00000483597.1:p.Ser32579=
|
|
NM_001256850.1:c.97737T>A
(TTN)
|
NP_001243779.1:p.Ser32579=
|
|
NM_001267550.2:c.102660T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34220=
|
|
NM_003319.4:c.75465T>A
(TTN)
|
NP_003310.4:p.Ser25155=
|
|
NM_133378.4:c.94956T>A
(TTN)
|
NP_596869.4:p.Ser31652=
|
|
NM_133432.3:c.75840T>A
(TTN)
|
NP_597676.3:p.Ser25280=
|
|
NM_133437.4:c.76041T>A
(TTN)
|
NP_597681.4:p.Ser25347=
|
|
NR_038271.1:n.446+10319A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-1777A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.101757T>A
(TTN)
|
XP_011510031.1:p.Ser33919=
|
|
XM_011511730.1:c.75651T>A
(TTN)
|
XP_011510032.1:p.Ser25217=
|
|
XM_011511731.1:c.75510T>A
(TTN)
|
XP_011510033.1:p.Ser25170=
|
|
XM_017004819.1:c.101553T>A
(TTN)
|
XP_016860308.1:p.Ser33851=
|
|
XM_017004820.1:c.96951T>A
(TTN)
|
XP_016860309.1:p.Ser32317=
|
|
XM_017004821.1:c.96948T>A
(TTN)
|
XP_016860310.1:p.Ser32316=
|
|
XM_017004822.1:c.93990T>A
(TTN)
|
XP_016860311.1:p.Ser31330=
|
|
XM_017004823.1:c.75606T>A
(TTN)
|
XP_016860312.1:p.Ser25202=
|
|
XM_024453094.1:c.97101T>A
(TTN)
|
XP_024308862.1:p.Ser32367=
|
|
XM_024453095.1:c.97098T>A
(TTN)
|
XP_024308863.1:p.Ser32366=
|
|
XM_024453096.1:c.96531T>A
(TTN)
|
XP_024308864.1:p.Ser32177=
|
|
XM_024453097.1:c.93873T>A
(TTN)
|
XP_024308865.1:p.Ser31291=
|
|
XM_024453098.1:c.93792T>A
(TTN)
|
XP_024308866.1:p.Ser31264=
|
|
XM_024453099.1:c.75555T>A
(TTN)
|
XP_024308867.1:p.Ser25185=
|
|
XM_024453100.1:c.65409T>A
(TTN)
|
XP_024308868.1:p.Ser21803=
|
|