ENST00000342992.11:c.83361A>G
(TTN)
|
ENSP00000343764.6:p.Glu27787=
|
|
ENST00000342175.11:c.64446A>G
(TTN)
|
ENSP00000340554.6:p.Glu21482=
|
|
ENST00000359218.10:c.64245A>G
(TTN)
|
ENSP00000352154.5:p.Glu21415=
|
|
ENST00000342175.10:c.64446A>G
(TTN)
|
ENSP00000340554.6:p.Glu21482=
|
|
ENST00000342992.10:c.83361A>G
(TTN)
|
ENSP00000343764.6:p.Glu27787=
|
|
ENST00000359218.9:c.64245A>G
(TTN)
|
ENSP00000352154.5:p.Glu21415=
|
|
ENST00000460472.6:c.63870A>G
(TTN)
|
ENSP00000434586.1:p.Glu21290=
|
|
ENST00000589042.5:c.91065A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu30355=
|
|
ENST00000591111.5:c.86142A>G
(TTN)
|
ENSP00000465570.1:p.Glu28714=
|
|
ENST00000615779.4:c.86142A>G
(TTN)
|
ENSP00000483597.1:p.Glu28714=
|
|
NM_001256850.1:c.86142A>G
(TTN)
|
NP_001243779.1:p.Glu28714=
|
|
NM_001267550.2:c.91065A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu30355=
|
|
NM_003319.4:c.63870A>G
(TTN)
|
NP_003310.4:p.Glu21290=
|
|
NM_133378.4:c.83361A>G
(TTN)
|
NP_596869.4:p.Glu27787=
|
|
NM_133432.3:c.64245A>G
(TTN)
|
NP_597676.3:p.Glu21415=
|
|
NM_133437.4:c.64446A>G
(TTN)
|
NP_597681.4:p.Glu21482=
|
|
NR_038271.1:n.447-19465T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9474T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.90162A>G
(TTN)
|
XP_011510031.1:p.Glu30054=
|
|
XM_011511730.1:c.64056A>G
(TTN)
|
XP_011510032.1:p.Glu21352=
|
|
XM_011511731.1:c.63915A>G
(TTN)
|
XP_011510033.1:p.Glu21305=
|
|
XM_017004819.1:c.89958A>G
(TTN)
|
XP_016860308.1:p.Glu29986=
|
|
XM_017004820.1:c.85356A>G
(TTN)
|
XP_016860309.1:p.Glu28452=
|
|
XM_017004821.1:c.85353A>G
(TTN)
|
XP_016860310.1:p.Glu28451=
|
|
XM_017004822.1:c.82395A>G
(TTN)
|
XP_016860311.1:p.Glu27465=
|
|
XM_017004823.1:c.64011A>G
(TTN)
|
XP_016860312.1:p.Glu21337=
|
|
XM_024453094.1:c.85506A>G
(TTN)
|
XP_024308862.1:p.Glu28502=
|
|
XM_024453095.1:c.85503A>G
(TTN)
|
XP_024308863.1:p.Glu28501=
|
|
XM_024453096.1:c.84936A>G
(TTN)
|
XP_024308864.1:p.Glu28312=
|
|
XM_024453097.1:c.82278A>G
(TTN)
|
XP_024308865.1:p.Glu27426=
|
|
XM_024453098.1:c.82197A>G
(TTN)
|
XP_024308866.1:p.Glu27399=
|
|
XM_024453099.1:c.63960A>G
(TTN)
|
XP_024308867.1:p.Glu21320=
|
|
XM_024453100.1:c.53814A>G
(TTN)
|
XP_024308868.1:p.Glu17938=
|
|