ENST00000342992.11:c.96742G>C
(TTN)
|
ENSP00000343764.6:p.Glu32248Gln
|
|
ENST00000342175.11:c.77827G>C
(TTN)
|
ENSP00000340554.6:p.Glu25943Gln
|
|
ENST00000359218.10:c.77626G>C
(TTN)
|
ENSP00000352154.5:p.Glu25876Gln
|
|
ENST00000342175.10:c.77827G>C
(TTN)
|
ENSP00000340554.6:p.Glu25943Gln
|
|
ENST00000342992.10:c.96742G>C
(TTN)
|
ENSP00000343764.6:p.Glu32248Gln
|
|
ENST00000359218.9:c.77626G>C
(TTN)
|
ENSP00000352154.5:p.Glu25876Gln
|
|
ENST00000460472.6:c.77251G>C
(TTN)
|
ENSP00000434586.1:p.Glu25751Gln
|
|
ENST00000589042.5:c.104446G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34816Gln
|
|
ENST00000591111.5:c.99523G>C
(TTN)
|
ENSP00000465570.1:p.Glu33175Gln
|
|
ENST00000615779.4:c.99523G>C
(TTN)
|
ENSP00000483597.1:p.Glu33175Gln
|
|
NM_001256850.1:c.99523G>C
(TTN)
|
NP_001243779.1:p.Glu33175Gln
|
|
NM_001267550.2:c.104446G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34816Gln
|
|
NM_003319.4:c.77251G>C
(TTN)
|
NP_003310.4:p.Glu25751Gln
|
|
NM_133378.4:c.96742G>C
(TTN)
|
NP_596869.4:p.Glu32248Gln
|
|
NM_133432.3:c.77626G>C
(TTN)
|
NP_597676.3:p.Glu25876Gln
|
|
NM_133437.4:c.77827G>C
(TTN)
|
NP_597681.4:p.Glu25943Gln
|
|
NR_038271.1:n.446+8533C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3563C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103543G>C
(TTN)
|
XP_011510031.1:p.Glu34515Gln
|
|
XM_011511730.1:c.77437G>C
(TTN)
|
XP_011510032.1:p.Glu25813Gln
|
|
XM_011511731.1:c.77296G>C
(TTN)
|
XP_011510033.1:p.Glu25766Gln
|
|
XM_017004819.1:c.103339G>C
(TTN)
|
XP_016860308.1:p.Glu34447Gln
|
|
XM_017004820.1:c.98737G>C
(TTN)
|
XP_016860309.1:p.Glu32913Gln
|
|
XM_017004821.1:c.98734G>C
(TTN)
|
XP_016860310.1:p.Glu32912Gln
|
|
XM_017004822.1:c.95776G>C
(TTN)
|
XP_016860311.1:p.Glu31926Gln
|
|
XM_017004823.1:c.77392G>C
(TTN)
|
XP_016860312.1:p.Glu25798Gln
|
|
XM_024453094.1:c.98887G>C
(TTN)
|
XP_024308862.1:p.Glu32963Gln
|
|
XM_024453095.1:c.98884G>C
(TTN)
|
XP_024308863.1:p.Glu32962Gln
|
|
XM_024453096.1:c.98317G>C
(TTN)
|
XP_024308864.1:p.Glu32773Gln
|
|
XM_024453097.1:c.95659G>C
(TTN)
|
XP_024308865.1:p.Glu31887Gln
|
|
XM_024453098.1:c.95578G>C
(TTN)
|
XP_024308866.1:p.Glu31860Gln
|
|
XM_024453099.1:c.77341G>C
(TTN)
|
XP_024308867.1:p.Glu25781Gln
|
|
XM_024453100.1:c.67195G>C
(TTN)
|
XP_024308868.1:p.Glu22399Gln
|
|