ENST00000342992.11:c.47356G>C
(TTN)
|
ENSP00000343764.6:p.Glu15786Gln
|
|
ENST00000342175.11:c.28441G>C
(TTN)
|
ENSP00000340554.6:p.Glu9481Gln
|
|
ENST00000359218.10:c.28240G>C
(TTN)
|
ENSP00000352154.5:p.Glu9414Gln
|
|
ENST00000342175.10:c.28441G>C
(TTN)
|
ENSP00000340554.6:p.Glu9481Gln
|
|
ENST00000342992.10:c.47356G>C
(TTN)
|
ENSP00000343764.6:p.Glu15786Gln
|
|
ENST00000359218.9:c.28240G>C
(TTN)
|
ENSP00000352154.5:p.Glu9414Gln
|
|
ENST00000460472.6:c.27865G>C
(TTN)
|
ENSP00000434586.1:p.Glu9289Gln
|
|
ENST00000589042.5:c.55060G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu18354Gln
|
|
ENST00000591111.5:c.50137G>C
(TTN)
|
ENSP00000465570.1:p.Glu16713Gln
|
|
ENST00000615779.4:c.50137G>C
(TTN)
|
ENSP00000483597.1:p.Glu16713Gln
|
|
NM_001256850.1:c.50137G>C
(TTN)
|
NP_001243779.1:p.Glu16713Gln
|
|
NM_001267550.2:c.55060G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu18354Gln
|
|
NM_003319.4:c.27865G>C
(TTN)
|
NP_003310.4:p.Glu9289Gln
|
|
NM_133378.4:c.47356G>C
(TTN)
|
NP_596869.4:p.Glu15786Gln
|
|
NM_133432.3:c.28240G>C
(TTN)
|
NP_597676.3:p.Glu9414Gln
|
|
NM_133437.4:c.28441G>C
(TTN)
|
NP_597681.4:p.Glu9481Gln
|
|
NR_038271.1:n.682+4661C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3917+1675C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.54157G>C
(TTN)
|
XP_011510031.1:p.Glu18053Gln
|
|
XM_011511730.1:c.28051G>C
(TTN)
|
XP_011510032.1:p.Glu9351Gln
|
|
XM_011511731.1:c.27910G>C
(TTN)
|
XP_011510033.1:p.Glu9304Gln
|
|
XM_017004819.1:c.53953G>C
(TTN)
|
XP_016860308.1:p.Glu17985Gln
|
|
XM_017004820.1:c.49351G>C
(TTN)
|
XP_016860309.1:p.Glu16451Gln
|
|
XM_017004821.1:c.49348G>C
(TTN)
|
XP_016860310.1:p.Glu16450Gln
|
|
XM_017004822.1:c.46390G>C
(TTN)
|
XP_016860311.1:p.Glu15464Gln
|
|
XM_017004823.1:c.28006G>C
(TTN)
|
XP_016860312.1:p.Glu9336Gln
|
|
XM_024453094.1:c.49501G>C
(TTN)
|
XP_024308862.1:p.Glu16501Gln
|
|
XM_024453095.1:c.49498G>C
(TTN)
|
XP_024308863.1:p.Glu16500Gln
|
|
XM_024453096.1:c.48931G>C
(TTN)
|
XP_024308864.1:p.Glu16311Gln
|
|
XM_024453097.1:c.46273G>C
(TTN)
|
XP_024308865.1:p.Glu15425Gln
|
|
XM_024453098.1:c.46192G>C
(TTN)
|
XP_024308866.1:p.Glu15398Gln
|
|
XM_024453099.1:c.27955G>C
(TTN)
|
XP_024308867.1:p.Glu9319Gln
|
|
XM_024453100.1:c.17809G>C
(TTN)
|
XP_024308868.1:p.Glu5937Gln
|
|