ENST00000342992.11:c.94955C>A
(TTN)
|
ENSP00000343764.6:p.Ser31652Tyr
|
|
ENST00000342175.11:c.76040C>A
(TTN)
|
ENSP00000340554.6:p.Ser25347Tyr
|
|
ENST00000359218.10:c.75839C>A
(TTN)
|
ENSP00000352154.5:p.Ser25280Tyr
|
|
ENST00000342175.10:c.76040C>A
(TTN)
|
ENSP00000340554.6:p.Ser25347Tyr
|
|
ENST00000342992.10:c.94955C>A
(TTN)
|
ENSP00000343764.6:p.Ser31652Tyr
|
|
ENST00000359218.9:c.75839C>A
(TTN)
|
ENSP00000352154.5:p.Ser25280Tyr
|
|
ENST00000460472.6:c.75464C>A
(TTN)
|
ENSP00000434586.1:p.Ser25155Tyr
|
|
ENST00000589042.5:c.102659C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34220Tyr
|
|
ENST00000591111.5:c.97736C>A
(TTN)
|
ENSP00000465570.1:p.Ser32579Tyr
|
|
ENST00000615779.4:c.97736C>A
(TTN)
|
ENSP00000483597.1:p.Ser32579Tyr
|
|
NM_001256850.1:c.97736C>A
(TTN)
|
NP_001243779.1:p.Ser32579Tyr
|
|
NM_001267550.2:c.102659C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34220Tyr
|
|
NM_003319.4:c.75464C>A
(TTN)
|
NP_003310.4:p.Ser25155Tyr
|
|
NM_133378.4:c.94955C>A
(TTN)
|
NP_596869.4:p.Ser31652Tyr
|
|
NM_133432.3:c.75839C>A
(TTN)
|
NP_597676.3:p.Ser25280Tyr
|
|
NM_133437.4:c.76040C>A
(TTN)
|
NP_597681.4:p.Ser25347Tyr
|
|
NR_038271.1:n.446+10320G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-1776G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.101756C>A
(TTN)
|
XP_011510031.1:p.Ser33919Tyr
|
|
XM_011511730.1:c.75650C>A
(TTN)
|
XP_011510032.1:p.Ser25217Tyr
|
|
XM_011511731.1:c.75509C>A
(TTN)
|
XP_011510033.1:p.Ser25170Tyr
|
|
XM_017004819.1:c.101552C>A
(TTN)
|
XP_016860308.1:p.Ser33851Tyr
|
|
XM_017004820.1:c.96950C>A
(TTN)
|
XP_016860309.1:p.Ser32317Tyr
|
|
XM_017004821.1:c.96947C>A
(TTN)
|
XP_016860310.1:p.Ser32316Tyr
|
|
XM_017004822.1:c.93989C>A
(TTN)
|
XP_016860311.1:p.Ser31330Tyr
|
|
XM_017004823.1:c.75605C>A
(TTN)
|
XP_016860312.1:p.Ser25202Tyr
|
|
XM_024453094.1:c.97100C>A
(TTN)
|
XP_024308862.1:p.Ser32367Tyr
|
|
XM_024453095.1:c.97097C>A
(TTN)
|
XP_024308863.1:p.Ser32366Tyr
|
|
XM_024453096.1:c.96530C>A
(TTN)
|
XP_024308864.1:p.Ser32177Tyr
|
|
XM_024453097.1:c.93872C>A
(TTN)
|
XP_024308865.1:p.Ser31291Tyr
|
|
XM_024453098.1:c.93791C>A
(TTN)
|
XP_024308866.1:p.Ser31264Tyr
|
|
XM_024453099.1:c.75554C>A
(TTN)
|
XP_024308867.1:p.Ser25185Tyr
|
|
XM_024453100.1:c.65408C>A
(TTN)
|
XP_024308868.1:p.Ser21803Tyr
|
|