ENST00000342992.11:c.67968A>T
(TTN)
|
ENSP00000343764.6:p.Leu22656=
|
|
ENST00000342175.11:c.49053A>T
(TTN)
|
ENSP00000340554.6:p.Leu16351=
|
|
ENST00000359218.10:c.48852A>T
(TTN)
|
ENSP00000352154.5:p.Leu16284=
|
|
ENST00000342175.10:c.49053A>T
(TTN)
|
ENSP00000340554.6:p.Leu16351=
|
|
ENST00000342992.10:c.67968A>T
(TTN)
|
ENSP00000343764.6:p.Leu22656=
|
|
ENST00000359218.9:c.48852A>T
(TTN)
|
ENSP00000352154.5:p.Leu16284=
|
|
ENST00000460472.6:c.48477A>T
(TTN)
|
ENSP00000434586.1:p.Leu16159=
|
|
ENST00000589042.5:c.75672A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu25224=
|
|
ENST00000591111.5:c.70749A>T
(TTN)
|
ENSP00000465570.1:p.Leu23583=
|
|
ENST00000615779.4:c.70749A>T
(TTN)
|
ENSP00000483597.1:p.Leu23583=
|
|
NM_001256850.1:c.70749A>T
(TTN)
|
NP_001243779.1:p.Leu23583=
|
|
NM_001267550.2:c.75672A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Leu25224=
|
|
NM_003319.4:c.48477A>T
(TTN)
|
NP_003310.4:p.Leu16159=
|
|
NM_133378.4:c.67968A>T
(TTN)
|
NP_596869.4:p.Leu22656=
|
|
NM_133432.3:c.48852A>T
(TTN)
|
NP_597676.3:p.Leu16284=
|
|
NM_133437.4:c.49053A>T
(TTN)
|
NP_597681.4:p.Leu16351=
|
|
NR_038271.1:n.447-840T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12112T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.74769A>T
(TTN)
|
XP_011510031.1:p.Leu24923=
|
|
XM_011511730.1:c.48663A>T
(TTN)
|
XP_011510032.1:p.Leu16221=
|
|
XM_011511731.1:c.48522A>T
(TTN)
|
XP_011510033.1:p.Leu16174=
|
|
XM_017004819.1:c.74565A>T
(TTN)
|
XP_016860308.1:p.Leu24855=
|
|
XM_017004820.1:c.69963A>T
(TTN)
|
XP_016860309.1:p.Leu23321=
|
|
XM_017004821.1:c.69960A>T
(TTN)
|
XP_016860310.1:p.Leu23320=
|
|
XM_017004822.1:c.67002A>T
(TTN)
|
XP_016860311.1:p.Leu22334=
|
|
XM_017004823.1:c.48618A>T
(TTN)
|
XP_016860312.1:p.Leu16206=
|
|
XM_024453094.1:c.70113A>T
(TTN)
|
XP_024308862.1:p.Leu23371=
|
|
XM_024453095.1:c.70110A>T
(TTN)
|
XP_024308863.1:p.Leu23370=
|
|
XM_024453096.1:c.69543A>T
(TTN)
|
XP_024308864.1:p.Leu23181=
|
|
XM_024453097.1:c.66885A>T
(TTN)
|
XP_024308865.1:p.Leu22295=
|
|
XM_024453098.1:c.66804A>T
(TTN)
|
XP_024308866.1:p.Leu22268=
|
|
XM_024453099.1:c.48567A>T
(TTN)
|
XP_024308867.1:p.Leu16189=
|
|
XM_024453100.1:c.38421A>T
(TTN)
|
XP_024308868.1:p.Leu12807=
|
|