ENST00000342992.11:c.82529C>A
(TTN)
|
ENSP00000343764.6:p.Ser27510Tyr
|
|
ENST00000342175.11:c.63614C>A
(TTN)
|
ENSP00000340554.6:p.Ser21205Tyr
|
|
ENST00000359218.10:c.63413C>A
(TTN)
|
ENSP00000352154.5:p.Ser21138Tyr
|
|
ENST00000342175.10:c.63614C>A
(TTN)
|
ENSP00000340554.6:p.Ser21205Tyr
|
|
ENST00000342992.10:c.82529C>A
(TTN)
|
ENSP00000343764.6:p.Ser27510Tyr
|
|
ENST00000359218.9:c.63413C>A
(TTN)
|
ENSP00000352154.5:p.Ser21138Tyr
|
|
ENST00000460472.6:c.63038C>A
(TTN)
|
ENSP00000434586.1:p.Ser21013Tyr
|
|
ENST00000589042.5:c.90233C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser30078Tyr
|
|
ENST00000591111.5:c.85310C>A
(TTN)
|
ENSP00000465570.1:p.Ser28437Tyr
|
|
ENST00000615779.4:c.85310C>A
(TTN)
|
ENSP00000483597.1:p.Ser28437Tyr
|
|
NM_001256850.1:c.85310C>A
(TTN)
|
NP_001243779.1:p.Ser28437Tyr
|
|
NM_001267550.2:c.90233C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser30078Tyr
|
|
NM_003319.4:c.63038C>A
(TTN)
|
NP_003310.4:p.Ser21013Tyr
|
|
NM_133378.4:c.82529C>A
(TTN)
|
NP_596869.4:p.Ser27510Tyr
|
|
NM_133432.3:c.63413C>A
(TTN)
|
NP_597676.3:p.Ser21138Tyr
|
|
NM_133437.4:c.63614C>A
(TTN)
|
NP_597681.4:p.Ser21205Tyr
|
|
NR_038271.1:n.447-18633G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10306G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.89330C>A
(TTN)
|
XP_011510031.1:p.Ser29777Tyr
|
|
XM_011511730.1:c.63224C>A
(TTN)
|
XP_011510032.1:p.Ser21075Tyr
|
|
XM_011511731.1:c.63083C>A
(TTN)
|
XP_011510033.1:p.Ser21028Tyr
|
|
XM_017004819.1:c.89126C>A
(TTN)
|
XP_016860308.1:p.Ser29709Tyr
|
|
XM_017004820.1:c.84524C>A
(TTN)
|
XP_016860309.1:p.Ser28175Tyr
|
|
XM_017004821.1:c.84521C>A
(TTN)
|
XP_016860310.1:p.Ser28174Tyr
|
|
XM_017004822.1:c.81563C>A
(TTN)
|
XP_016860311.1:p.Ser27188Tyr
|
|
XM_017004823.1:c.63179C>A
(TTN)
|
XP_016860312.1:p.Ser21060Tyr
|
|
XM_024453094.1:c.84674C>A
(TTN)
|
XP_024308862.1:p.Ser28225Tyr
|
|
XM_024453095.1:c.84671C>A
(TTN)
|
XP_024308863.1:p.Ser28224Tyr
|
|
XM_024453096.1:c.84104C>A
(TTN)
|
XP_024308864.1:p.Ser28035Tyr
|
|
XM_024453097.1:c.81446C>A
(TTN)
|
XP_024308865.1:p.Ser27149Tyr
|
|
XM_024453098.1:c.81365C>A
(TTN)
|
XP_024308866.1:p.Ser27122Tyr
|
|
XM_024453099.1:c.63128C>A
(TTN)
|
XP_024308867.1:p.Ser21043Tyr
|
|
XM_024453100.1:c.52982C>A
(TTN)
|
XP_024308868.1:p.Ser17661Tyr
|
|