ENST00000342992.11:c.99869C>A
(TTN)
|
ENSP00000343764.6:p.Ser33290Tyr
|
|
ENST00000342175.11:c.80954C>A
(TTN)
|
ENSP00000340554.6:p.Ser26985Tyr
|
|
ENST00000359218.10:c.80753C>A
(TTN)
|
ENSP00000352154.5:p.Ser26918Tyr
|
|
ENST00000342175.10:c.80954C>A
(TTN)
|
ENSP00000340554.6:p.Ser26985Tyr
|
|
ENST00000342992.10:c.99869C>A
(TTN)
|
ENSP00000343764.6:p.Ser33290Tyr
|
|
ENST00000359218.9:c.80753C>A
(TTN)
|
ENSP00000352154.5:p.Ser26918Tyr
|
|
ENST00000460472.6:c.80378C>A
(TTN)
|
ENSP00000434586.1:p.Ser26793Tyr
|
|
ENST00000589042.5:c.107573C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser35858Tyr
|
|
ENST00000591111.5:c.102650C>A
(TTN)
|
ENSP00000465570.1:p.Ser34217Tyr
|
|
ENST00000615779.4:c.102650C>A
(TTN)
|
ENSP00000483597.1:p.Ser34217Tyr
|
|
NM_001256850.1:c.102650C>A
(TTN)
|
NP_001243779.1:p.Ser34217Tyr
|
|
NM_001267550.2:c.107573C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser35858Tyr
|
|
NM_003319.4:c.80378C>A
(TTN)
|
NP_003310.4:p.Ser26793Tyr
|
|
NM_133378.4:c.99869C>A
(TTN)
|
NP_596869.4:p.Ser33290Tyr
|
|
NM_133432.3:c.80753C>A
(TTN)
|
NP_597676.3:p.Ser26918Tyr
|
|
NM_133437.4:c.80954C>A
(TTN)
|
NP_597681.4:p.Ser26985Tyr
|
|
NR_038271.1:n.446+3917G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3917G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.106670C>A
(TTN)
|
XP_011510031.1:p.Ser35557Tyr
|
|
XM_011511730.1:c.80564C>A
(TTN)
|
XP_011510032.1:p.Ser26855Tyr
|
|
XM_011511731.1:c.80423C>A
(TTN)
|
XP_011510033.1:p.Ser26808Tyr
|
|
XM_017004819.1:c.106466C>A
(TTN)
|
XP_016860308.1:p.Ser35489Tyr
|
|
XM_017004820.1:c.101864C>A
(TTN)
|
XP_016860309.1:p.Ser33955Tyr
|
|
XM_017004821.1:c.101861C>A
(TTN)
|
XP_016860310.1:p.Ser33954Tyr
|
|
XM_017004822.1:c.98903C>A
(TTN)
|
XP_016860311.1:p.Ser32968Tyr
|
|
XM_017004823.1:c.80519C>A
(TTN)
|
XP_016860312.1:p.Ser26840Tyr
|
|
XM_024453094.1:c.102014C>A
(TTN)
|
XP_024308862.1:p.Ser34005Tyr
|
|
XM_024453095.1:c.102011C>A
(TTN)
|
XP_024308863.1:p.Ser34004Tyr
|
|
XM_024453096.1:c.101444C>A
(TTN)
|
XP_024308864.1:p.Ser33815Tyr
|
|
XM_024453097.1:c.98786C>A
(TTN)
|
XP_024308865.1:p.Ser32929Tyr
|
|
XM_024453098.1:c.98705C>A
(TTN)
|
XP_024308866.1:p.Ser32902Tyr
|
|
XM_024453099.1:c.80468C>A
(TTN)
|
XP_024308867.1:p.Ser26823Tyr
|
|
XM_024453100.1:c.70322C>A
(TTN)
|
XP_024308868.1:p.Ser23441Tyr
|
|