ENST00000342992.11:c.73812C>T
(TTN)
|
ENSP00000343764.6:p.Asp24604=
|
|
ENST00000342175.11:c.54897C>T
(TTN)
|
ENSP00000340554.6:p.Asp18299=
|
|
ENST00000359218.10:c.54696C>T
(TTN)
|
ENSP00000352154.5:p.Asp18232=
|
|
ENST00000342175.10:c.54897C>T
(TTN)
|
ENSP00000340554.6:p.Asp18299=
|
|
ENST00000342992.10:c.73812C>T
(TTN)
|
ENSP00000343764.6:p.Asp24604=
|
|
ENST00000359218.9:c.54696C>T
(TTN)
|
ENSP00000352154.5:p.Asp18232=
|
|
ENST00000460472.6:c.54321C>T
(TTN)
|
ENSP00000434586.1:p.Asp18107=
|
|
ENST00000589042.5:c.81516C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asp27172=
|
|
ENST00000591111.5:c.76593C>T
(TTN)
|
ENSP00000465570.1:p.Asp25531=
|
|
ENST00000615779.4:c.76593C>T
(TTN)
|
ENSP00000483597.1:p.Asp25531=
|
|
NM_001256850.1:c.76593C>T
(TTN)
|
NP_001243779.1:p.Asp25531=
|
|
NM_001267550.2:c.81516C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asp27172=
|
|
NM_003319.4:c.54321C>T
(TTN)
|
NP_003310.4:p.Asp18107=
|
|
NM_133378.4:c.73812C>T
(TTN)
|
NP_596869.4:p.Asp24604=
|
|
NM_133432.3:c.54696C>T
(TTN)
|
NP_597676.3:p.Asp18232=
|
|
NM_133437.4:c.54897C>T
(TTN)
|
NP_597681.4:p.Asp18299=
|
|
NR_038271.1:n.447-6684G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-17956G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.80613C>T
(TTN)
|
XP_011510031.1:p.Asp26871=
|
|
XM_011511730.1:c.54507C>T
(TTN)
|
XP_011510032.1:p.Asp18169=
|
|
XM_011511731.1:c.54366C>T
(TTN)
|
XP_011510033.1:p.Asp18122=
|
|
XM_017004819.1:c.80409C>T
(TTN)
|
XP_016860308.1:p.Asp26803=
|
|
XM_017004820.1:c.75807C>T
(TTN)
|
XP_016860309.1:p.Asp25269=
|
|
XM_017004821.1:c.75804C>T
(TTN)
|
XP_016860310.1:p.Asp25268=
|
|
XM_017004822.1:c.72846C>T
(TTN)
|
XP_016860311.1:p.Asp24282=
|
|
XM_017004823.1:c.54462C>T
(TTN)
|
XP_016860312.1:p.Asp18154=
|
|
XM_024453094.1:c.75957C>T
(TTN)
|
XP_024308862.1:p.Asp25319=
|
|
XM_024453095.1:c.75954C>T
(TTN)
|
XP_024308863.1:p.Asp25318=
|
|
XM_024453096.1:c.75387C>T
(TTN)
|
XP_024308864.1:p.Asp25129=
|
|
XM_024453097.1:c.72729C>T
(TTN)
|
XP_024308865.1:p.Asp24243=
|
|
XM_024453098.1:c.72648C>T
(TTN)
|
XP_024308866.1:p.Asp24216=
|
|
XM_024453099.1:c.54411C>T
(TTN)
|
XP_024308867.1:p.Asp18137=
|
|
XM_024453100.1:c.44265C>T
(TTN)
|
XP_024308868.1:p.Asp14755=
|
|