ENST00000342992.11:c.98739G>A
(TTN)
|
ENSP00000343764.6:p.Lys32913=
|
|
ENST00000342175.11:c.79824G>A
(TTN)
|
ENSP00000340554.6:p.Lys26608=
|
|
ENST00000359218.10:c.79623G>A
(TTN)
|
ENSP00000352154.5:p.Lys26541=
|
|
ENST00000342175.10:c.79824G>A
(TTN)
|
ENSP00000340554.6:p.Lys26608=
|
|
ENST00000342992.10:c.98739G>A
(TTN)
|
ENSP00000343764.6:p.Lys32913=
|
|
ENST00000359218.9:c.79623G>A
(TTN)
|
ENSP00000352154.5:p.Lys26541=
|
|
ENST00000460472.6:c.79248G>A
(TTN)
|
ENSP00000434586.1:p.Lys26416=
|
|
ENST00000589042.5:c.106443G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys35481=
|
|
ENST00000591111.5:c.101520G>A
(TTN)
|
ENSP00000465570.1:p.Lys33840=
|
|
ENST00000615779.4:c.101520G>A
(TTN)
|
ENSP00000483597.1:p.Lys33840=
|
|
NM_001256850.1:c.101520G>A
(TTN)
|
NP_001243779.1:p.Lys33840=
|
|
NM_001267550.2:c.106443G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Lys35481=
|
|
NM_003319.4:c.79248G>A
(TTN)
|
NP_003310.4:p.Lys26416=
|
|
NM_133378.4:c.98739G>A
(TTN)
|
NP_596869.4:p.Lys32913=
|
|
NM_133432.3:c.79623G>A
(TTN)
|
NP_597676.3:p.Lys26541=
|
|
NM_133437.4:c.79824G>A
(TTN)
|
NP_597681.4:p.Lys26608=
|
|
NR_038271.1:n.446+6412C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5684C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105540G>A
(TTN)
|
XP_011510031.1:p.Lys35180=
|
|
XM_011511730.1:c.79434G>A
(TTN)
|
XP_011510032.1:p.Lys26478=
|
|
XM_011511731.1:c.79293G>A
(TTN)
|
XP_011510033.1:p.Lys26431=
|
|
XM_017004819.1:c.105336G>A
(TTN)
|
XP_016860308.1:p.Lys35112=
|
|
XM_017004820.1:c.100734G>A
(TTN)
|
XP_016860309.1:p.Lys33578=
|
|
XM_017004821.1:c.100731G>A
(TTN)
|
XP_016860310.1:p.Lys33577=
|
|
XM_017004822.1:c.97773G>A
(TTN)
|
XP_016860311.1:p.Lys32591=
|
|
XM_017004823.1:c.79389G>A
(TTN)
|
XP_016860312.1:p.Lys26463=
|
|
XM_024453094.1:c.100884G>A
(TTN)
|
XP_024308862.1:p.Lys33628=
|
|
XM_024453095.1:c.100881G>A
(TTN)
|
XP_024308863.1:p.Lys33627=
|
|
XM_024453096.1:c.100314G>A
(TTN)
|
XP_024308864.1:p.Lys33438=
|
|
XM_024453097.1:c.97656G>A
(TTN)
|
XP_024308865.1:p.Lys32552=
|
|
XM_024453098.1:c.97575G>A
(TTN)
|
XP_024308866.1:p.Lys32525=
|
|
XM_024453099.1:c.79338G>A
(TTN)
|
XP_024308867.1:p.Lys26446=
|
|
XM_024453100.1:c.69192G>A
(TTN)
|
XP_024308868.1:p.Lys23064=
|
|