ENST00000342992.11:c.78794C>A
(TTN)
|
ENSP00000343764.6:p.Ala26265Asp
|
|
ENST00000342175.11:c.59879C>A
(TTN)
|
ENSP00000340554.6:p.Ala19960Asp
|
|
ENST00000359218.10:c.59678C>A
(TTN)
|
ENSP00000352154.5:p.Ala19893Asp
|
|
ENST00000342175.10:c.59879C>A
(TTN)
|
ENSP00000340554.6:p.Ala19960Asp
|
|
ENST00000342992.10:c.78794C>A
(TTN)
|
ENSP00000343764.6:p.Ala26265Asp
|
|
ENST00000359218.9:c.59678C>A
(TTN)
|
ENSP00000352154.5:p.Ala19893Asp
|
|
ENST00000460472.6:c.59303C>A
(TTN)
|
ENSP00000434586.1:p.Ala19768Asp
|
|
ENST00000589042.5:c.86498C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala28833Asp
|
|
ENST00000591111.5:c.81575C>A
(TTN)
|
ENSP00000465570.1:p.Ala27192Asp
|
|
ENST00000615779.4:c.81575C>A
(TTN)
|
ENSP00000483597.1:p.Ala27192Asp
|
|
NM_001256850.1:c.81575C>A
(TTN)
|
NP_001243779.1:p.Ala27192Asp
|
|
NM_001267550.2:c.86498C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala28833Asp
|
|
NM_003319.4:c.59303C>A
(TTN)
|
NP_003310.4:p.Ala19768Asp
|
|
NM_133378.4:c.78794C>A
(TTN)
|
NP_596869.4:p.Ala26265Asp
|
|
NM_133432.3:c.59678C>A
(TTN)
|
NP_597676.3:p.Ala19893Asp
|
|
NM_133437.4:c.59879C>A
(TTN)
|
NP_597681.4:p.Ala19960Asp
|
|
NR_038271.1:n.447-11666G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17273G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.85595C>A
(TTN)
|
XP_011510031.1:p.Ala28532Asp
|
|
XM_011511730.1:c.59489C>A
(TTN)
|
XP_011510032.1:p.Ala19830Asp
|
|
XM_011511731.1:c.59348C>A
(TTN)
|
XP_011510033.1:p.Ala19783Asp
|
|
XM_017004819.1:c.85391C>A
(TTN)
|
XP_016860308.1:p.Ala28464Asp
|
|
XM_017004820.1:c.80789C>A
(TTN)
|
XP_016860309.1:p.Ala26930Asp
|
|
XM_017004821.1:c.80786C>A
(TTN)
|
XP_016860310.1:p.Ala26929Asp
|
|
XM_017004822.1:c.77828C>A
(TTN)
|
XP_016860311.1:p.Ala25943Asp
|
|
XM_017004823.1:c.59444C>A
(TTN)
|
XP_016860312.1:p.Ala19815Asp
|
|
XM_024453094.1:c.80939C>A
(TTN)
|
XP_024308862.1:p.Ala26980Asp
|
|
XM_024453095.1:c.80936C>A
(TTN)
|
XP_024308863.1:p.Ala26979Asp
|
|
XM_024453096.1:c.80369C>A
(TTN)
|
XP_024308864.1:p.Ala26790Asp
|
|
XM_024453097.1:c.77711C>A
(TTN)
|
XP_024308865.1:p.Ala25904Asp
|
|
XM_024453098.1:c.77630C>A
(TTN)
|
XP_024308866.1:p.Ala25877Asp
|
|
XM_024453099.1:c.59393C>A
(TTN)
|
XP_024308867.1:p.Ala19798Asp
|
|
XM_024453100.1:c.49247C>A
(TTN)
|
XP_024308868.1:p.Ala16416Asp
|
|