ENST00000342992.11:c.51362C>T
(TTN)
|
ENSP00000343764.6:p.Ala17121Val
|
|
ENST00000342175.11:c.32447C>T
(TTN)
|
ENSP00000340554.6:p.Ala10816Val
|
|
ENST00000359218.10:c.32246C>T
(TTN)
|
ENSP00000352154.5:p.Ala10749Val
|
|
ENST00000342175.10:c.32447C>T
(TTN)
|
ENSP00000340554.6:p.Ala10816Val
|
|
ENST00000342992.10:c.51362C>T
(TTN)
|
ENSP00000343764.6:p.Ala17121Val
|
|
ENST00000359218.9:c.32246C>T
(TTN)
|
ENSP00000352154.5:p.Ala10749Val
|
|
ENST00000460472.6:c.31871C>T
(TTN)
|
ENSP00000434586.1:p.Ala10624Val
|
|
ENST00000589042.5:c.59066C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala19689Val
|
|
ENST00000591111.5:c.54143C>T
(TTN)
|
ENSP00000465570.1:p.Ala18048Val
|
|
ENST00000615779.4:c.54143C>T
(TTN)
|
ENSP00000483597.1:p.Ala18048Val
|
|
NM_001256850.1:c.54143C>T
(TTN)
|
NP_001243779.1:p.Ala18048Val
|
|
NM_001267550.2:c.59066C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala19689Val
|
|
NM_003319.4:c.31871C>T
(TTN)
|
NP_003310.4:p.Ala10624Val
|
|
NM_133378.4:c.51362C>T
(TTN)
|
NP_596869.4:p.Ala17121Val
|
|
NM_133432.3:c.32246C>T
(TTN)
|
NP_597676.3:p.Ala10749Val
|
|
NM_133437.4:c.32447C>T
(TTN)
|
NP_597681.4:p.Ala10816Val
|
|
NR_038271.1:n.597-4543G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+1739G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.58163C>T
(TTN)
|
XP_011510031.1:p.Ala19388Val
|
|
XM_011511730.1:c.32057C>T
(TTN)
|
XP_011510032.1:p.Ala10686Val
|
|
XM_011511731.1:c.31916C>T
(TTN)
|
XP_011510033.1:p.Ala10639Val
|
|
XM_017004819.1:c.57959C>T
(TTN)
|
XP_016860308.1:p.Ala19320Val
|
|
XM_017004820.1:c.53357C>T
(TTN)
|
XP_016860309.1:p.Ala17786Val
|
|
XM_017004821.1:c.53354C>T
(TTN)
|
XP_016860310.1:p.Ala17785Val
|
|
XM_017004822.1:c.50396C>T
(TTN)
|
XP_016860311.1:p.Ala16799Val
|
|
XM_017004823.1:c.32012C>T
(TTN)
|
XP_016860312.1:p.Ala10671Val
|
|
XM_024453094.1:c.53507C>T
(TTN)
|
XP_024308862.1:p.Ala17836Val
|
|
XM_024453095.1:c.53504C>T
(TTN)
|
XP_024308863.1:p.Ala17835Val
|
|
XM_024453096.1:c.52937C>T
(TTN)
|
XP_024308864.1:p.Ala17646Val
|
|
XM_024453097.1:c.50279C>T
(TTN)
|
XP_024308865.1:p.Ala16760Val
|
|
XM_024453098.1:c.50198C>T
(TTN)
|
XP_024308866.1:p.Ala16733Val
|
|
XM_024453099.1:c.31961C>T
(TTN)
|
XP_024308867.1:p.Ala10654Val
|
|
XM_024453100.1:c.21815C>T
(TTN)
|
XP_024308868.1:p.Ala7272Val
|
|