ENST00000342992.11:c.39597C>A
(TTN)
|
ENSP00000343764.6:p.Ile13199=
|
|
ENST00000342175.11:c.20682C>A
(TTN)
|
ENSP00000340554.6:p.Ile6894=
|
|
ENST00000359218.10:c.20481C>A
(TTN)
|
ENSP00000352154.5:p.Ile6827=
|
|
ENST00000342175.10:c.20682C>A
(TTN)
|
ENSP00000340554.6:p.Ile6894=
|
|
ENST00000342992.10:c.39597C>A
(TTN)
|
ENSP00000343764.6:p.Ile13199=
|
|
ENST00000359218.9:c.20481C>A
(TTN)
|
ENSP00000352154.5:p.Ile6827=
|
|
ENST00000460472.6:c.20106C>A
(TTN)
|
ENSP00000434586.1:p.Ile6702=
|
|
ENST00000589042.5:c.47301C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile15767=
|
|
ENST00000591111.5:c.42378C>A
(TTN)
|
ENSP00000465570.1:p.Ile14126=
|
|
ENST00000615779.4:c.42378C>A
(TTN)
|
ENSP00000483597.1:p.Ile14126=
|
|
NM_001256850.1:c.42378C>A
(TTN)
|
NP_001243779.1:p.Ile14126=
|
|
NM_001267550.2:c.47301C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ile15767=
|
|
NM_003319.4:c.20106C>A
(TTN)
|
NP_003310.4:p.Ile6702=
|
|
NM_133378.4:c.39597C>A
(TTN)
|
NP_596869.4:p.Ile13199=
|
|
NM_133432.3:c.20481C>A
(TTN)
|
NP_597676.3:p.Ile6827=
|
|
NM_133437.4:c.20682C>A
(TTN)
|
NP_597681.4:p.Ile6894=
|
|
NR_038271.1:n.1605-1703G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.46398C>A
(TTN)
|
XP_011510031.1:p.Ile15466=
|
|
XM_011511730.1:c.20292C>A
(TTN)
|
XP_011510032.1:p.Ile6764=
|
|
XM_011511731.1:c.20151C>A
(TTN)
|
XP_011510033.1:p.Ile6717=
|
|
XM_017004819.1:c.46194C>A
(TTN)
|
XP_016860308.1:p.Ile15398=
|
|
XM_017004820.1:c.41592C>A
(TTN)
|
XP_016860309.1:p.Ile13864=
|
|
XM_017004821.1:c.41589C>A
(TTN)
|
XP_016860310.1:p.Ile13863=
|
|
XM_017004822.1:c.38631C>A
(TTN)
|
XP_016860311.1:p.Ile12877=
|
|
XM_017004823.1:c.20247C>A
(TTN)
|
XP_016860312.1:p.Ile6749=
|
|
XM_024453094.1:c.41742C>A
(TTN)
|
XP_024308862.1:p.Ile13914=
|
|
XM_024453095.1:c.41739C>A
(TTN)
|
XP_024308863.1:p.Ile13913=
|
|
XM_024453096.1:c.41172C>A
(TTN)
|
XP_024308864.1:p.Ile13724=
|
|
XM_024453097.1:c.38514C>A
(TTN)
|
XP_024308865.1:p.Ile12838=
|
|
XM_024453098.1:c.38433C>A
(TTN)
|
XP_024308866.1:p.Ile12811=
|
|
XM_024453099.1:c.20196C>A
(TTN)
|
XP_024308867.1:p.Ile6732=
|
|
XM_024453100.1:c.10050C>A
(TTN)
|
XP_024308868.1:p.Ile3350=
|
|