ENST00000342992.11:c.88102G>C
(TTN)
|
ENSP00000343764.6:p.Asp29368His
|
|
ENST00000342175.11:c.69187G>C
(TTN)
|
ENSP00000340554.6:p.Asp23063His
|
|
ENST00000359218.10:c.68986G>C
(TTN)
|
ENSP00000352154.5:p.Asp22996His
|
|
ENST00000342175.10:c.69187G>C
(TTN)
|
ENSP00000340554.6:p.Asp23063His
|
|
ENST00000342992.10:c.88102G>C
(TTN)
|
ENSP00000343764.6:p.Asp29368His
|
|
ENST00000359218.9:c.68986G>C
(TTN)
|
ENSP00000352154.5:p.Asp22996His
|
|
ENST00000460472.6:c.68611G>C
(TTN)
|
ENSP00000434586.1:p.Asp22871His
|
|
ENST00000589042.5:c.95806G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp31936His
|
|
ENST00000591111.5:c.90883G>C
(TTN)
|
ENSP00000465570.1:p.Asp30295His
|
|
ENST00000615779.4:c.90883G>C
(TTN)
|
ENSP00000483597.1:p.Asp30295His
|
|
NM_001256850.1:c.90883G>C
(TTN)
|
NP_001243779.1:p.Asp30295His
|
|
NM_001267550.2:c.95806G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asp31936His
|
|
NM_003319.4:c.68611G>C
(TTN)
|
NP_003310.4:p.Asp22871His
|
|
NM_133378.4:c.88102G>C
(TTN)
|
NP_596869.4:p.Asp29368His
|
|
NM_133432.3:c.68986G>C
(TTN)
|
NP_597676.3:p.Asp22996His
|
|
NM_133437.4:c.69187G>C
(TTN)
|
NP_597681.4:p.Asp23063His
|
|
NR_038271.1:n.446+20787C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+2062C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.94903G>C
(TTN)
|
XP_011510031.1:p.Asp31635His
|
|
XM_011511730.1:c.68797G>C
(TTN)
|
XP_011510032.1:p.Asp22933His
|
|
XM_011511731.1:c.68656G>C
(TTN)
|
XP_011510033.1:p.Asp22886His
|
|
XM_017004819.1:c.94699G>C
(TTN)
|
XP_016860308.1:p.Asp31567His
|
|
XM_017004820.1:c.90097G>C
(TTN)
|
XP_016860309.1:p.Asp30033His
|
|
XM_017004821.1:c.90094G>C
(TTN)
|
XP_016860310.1:p.Asp30032His
|
|
XM_017004822.1:c.87136G>C
(TTN)
|
XP_016860311.1:p.Asp29046His
|
|
XM_017004823.1:c.68752G>C
(TTN)
|
XP_016860312.1:p.Asp22918His
|
|
XM_024453094.1:c.90247G>C
(TTN)
|
XP_024308862.1:p.Asp30083His
|
|
XM_024453095.1:c.90244G>C
(TTN)
|
XP_024308863.1:p.Asp30082His
|
|
XM_024453096.1:c.89677G>C
(TTN)
|
XP_024308864.1:p.Asp29893His
|
|
XM_024453097.1:c.87019G>C
(TTN)
|
XP_024308865.1:p.Asp29007His
|
|
XM_024453098.1:c.86938G>C
(TTN)
|
XP_024308866.1:p.Asp28980His
|
|
XM_024453099.1:c.68701G>C
(TTN)
|
XP_024308867.1:p.Asp22901His
|
|
XM_024453100.1:c.58555G>C
(TTN)
|
XP_024308868.1:p.Asp19519His
|
|