ENST00000342992.11:c.88958T>G
(TTN)
|
ENSP00000343764.6:p.Leu29653Arg
|
|
ENST00000342175.11:c.70043T>G
(TTN)
|
ENSP00000340554.6:p.Leu23348Arg
|
|
ENST00000359218.10:c.69842T>G
(TTN)
|
ENSP00000352154.5:p.Leu23281Arg
|
|
ENST00000342175.10:c.70043T>G
(TTN)
|
ENSP00000340554.6:p.Leu23348Arg
|
|
ENST00000342992.10:c.88958T>G
(TTN)
|
ENSP00000343764.6:p.Leu29653Arg
|
|
ENST00000359218.9:c.69842T>G
(TTN)
|
ENSP00000352154.5:p.Leu23281Arg
|
|
ENST00000460472.6:c.69467T>G
(TTN)
|
ENSP00000434586.1:p.Leu23156Arg
|
|
ENST00000589042.5:c.96662T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu32221Arg
|
|
ENST00000591111.5:c.91739T>G
(TTN)
|
ENSP00000465570.1:p.Leu30580Arg
|
|
ENST00000615779.4:c.91739T>G
(TTN)
|
ENSP00000483597.1:p.Leu30580Arg
|
|
NM_001256850.1:c.91739T>G
(TTN)
|
NP_001243779.1:p.Leu30580Arg
|
|
NM_001267550.2:c.96662T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Leu32221Arg
|
|
NM_003319.4:c.69467T>G
(TTN)
|
NP_003310.4:p.Leu23156Arg
|
|
NM_133378.4:c.88958T>G
(TTN)
|
NP_596869.4:p.Leu29653Arg
|
|
NM_133432.3:c.69842T>G
(TTN)
|
NP_597676.3:p.Leu23281Arg
|
|
NM_133437.4:c.70043T>G
(TTN)
|
NP_597681.4:p.Leu23348Arg
|
|
NR_038271.1:n.446+19675A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+950A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.95759T>G
(TTN)
|
XP_011510031.1:p.Leu31920Arg
|
|
XM_011511730.1:c.69653T>G
(TTN)
|
XP_011510032.1:p.Leu23218Arg
|
|
XM_011511731.1:c.69512T>G
(TTN)
|
XP_011510033.1:p.Leu23171Arg
|
|
XM_017004819.1:c.95555T>G
(TTN)
|
XP_016860308.1:p.Leu31852Arg
|
|
XM_017004820.1:c.90953T>G
(TTN)
|
XP_016860309.1:p.Leu30318Arg
|
|
XM_017004821.1:c.90950T>G
(TTN)
|
XP_016860310.1:p.Leu30317Arg
|
|
XM_017004822.1:c.87992T>G
(TTN)
|
XP_016860311.1:p.Leu29331Arg
|
|
XM_017004823.1:c.69608T>G
(TTN)
|
XP_016860312.1:p.Leu23203Arg
|
|
XM_024453094.1:c.91103T>G
(TTN)
|
XP_024308862.1:p.Leu30368Arg
|
|
XM_024453095.1:c.91100T>G
(TTN)
|
XP_024308863.1:p.Leu30367Arg
|
|
XM_024453096.1:c.90533T>G
(TTN)
|
XP_024308864.1:p.Leu30178Arg
|
|
XM_024453097.1:c.87875T>G
(TTN)
|
XP_024308865.1:p.Leu29292Arg
|
|
XM_024453098.1:c.87794T>G
(TTN)
|
XP_024308866.1:p.Leu29265Arg
|
|
XM_024453099.1:c.69557T>G
(TTN)
|
XP_024308867.1:p.Leu23186Arg
|
|
XM_024453100.1:c.59411T>G
(TTN)
|
XP_024308868.1:p.Leu19804Arg
|
|