ENST00000342992.11:c.88351G>C
(TTN)
|
ENSP00000343764.6:p.Asp29451His
|
|
ENST00000342175.11:c.69436G>C
(TTN)
|
ENSP00000340554.6:p.Asp23146His
|
|
ENST00000359218.10:c.69235G>C
(TTN)
|
ENSP00000352154.5:p.Asp23079His
|
|
ENST00000342175.10:c.69436G>C
(TTN)
|
ENSP00000340554.6:p.Asp23146His
|
|
ENST00000342992.10:c.88351G>C
(TTN)
|
ENSP00000343764.6:p.Asp29451His
|
|
ENST00000359218.9:c.69235G>C
(TTN)
|
ENSP00000352154.5:p.Asp23079His
|
|
ENST00000460472.6:c.68860G>C
(TTN)
|
ENSP00000434586.1:p.Asp22954His
|
|
ENST00000589042.5:c.96055G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp32019His
|
|
ENST00000591111.5:c.91132G>C
(TTN)
|
ENSP00000465570.1:p.Asp30378His
|
|
ENST00000615779.4:c.91132G>C
(TTN)
|
ENSP00000483597.1:p.Asp30378His
|
|
NM_001256850.1:c.91132G>C
(TTN)
|
NP_001243779.1:p.Asp30378His
|
|
NM_001267550.2:c.96055G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp32019His
|
|
NM_003319.4:c.68860G>C
(TTN)
|
NP_003310.4:p.Asp22954His
|
|
NM_133378.4:c.88351G>C
(TTN)
|
NP_596869.4:p.Asp29451His
|
|
NM_133432.3:c.69235G>C
(TTN)
|
NP_597676.3:p.Asp23079His
|
|
NM_133437.4:c.69436G>C
(TTN)
|
NP_597681.4:p.Asp23146His
|
|
NR_038271.1:n.446+20453C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+1728C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.95152G>C
(TTN)
|
XP_011510031.1:p.Asp31718His
|
|
XM_011511730.1:c.69046G>C
(TTN)
|
XP_011510032.1:p.Asp23016His
|
|
XM_011511731.1:c.68905G>C
(TTN)
|
XP_011510033.1:p.Asp22969His
|
|
XM_017004819.1:c.94948G>C
(TTN)
|
XP_016860308.1:p.Asp31650His
|
|
XM_017004820.1:c.90346G>C
(TTN)
|
XP_016860309.1:p.Asp30116His
|
|
XM_017004821.1:c.90343G>C
(TTN)
|
XP_016860310.1:p.Asp30115His
|
|
XM_017004822.1:c.87385G>C
(TTN)
|
XP_016860311.1:p.Asp29129His
|
|
XM_017004823.1:c.69001G>C
(TTN)
|
XP_016860312.1:p.Asp23001His
|
|
XM_024453094.1:c.90496G>C
(TTN)
|
XP_024308862.1:p.Asp30166His
|
|
XM_024453095.1:c.90493G>C
(TTN)
|
XP_024308863.1:p.Asp30165His
|
|
XM_024453096.1:c.89926G>C
(TTN)
|
XP_024308864.1:p.Asp29976His
|
|
XM_024453097.1:c.87268G>C
(TTN)
|
XP_024308865.1:p.Asp29090His
|
|
XM_024453098.1:c.87187G>C
(TTN)
|
XP_024308866.1:p.Asp29063His
|
|
XM_024453099.1:c.68950G>C
(TTN)
|
XP_024308867.1:p.Asp22984His
|
|
XM_024453100.1:c.58804G>C
(TTN)
|
XP_024308868.1:p.Asp19602His
|
|