ENST00000342992.11:c.92970A>T
(TTN)
|
ENSP00000343764.6:p.Ala30990=
|
|
ENST00000342175.11:c.74055A>T
(TTN)
|
ENSP00000340554.6:p.Ala24685=
|
|
ENST00000359218.10:c.73854A>T
(TTN)
|
ENSP00000352154.5:p.Ala24618=
|
|
ENST00000342175.10:c.74055A>T
(TTN)
|
ENSP00000340554.6:p.Ala24685=
|
|
ENST00000342992.10:c.92970A>T
(TTN)
|
ENSP00000343764.6:p.Ala30990=
|
|
ENST00000359218.9:c.73854A>T
(TTN)
|
ENSP00000352154.5:p.Ala24618=
|
|
ENST00000460472.6:c.73479A>T
(TTN)
|
ENSP00000434586.1:p.Ala24493=
|
|
ENST00000589042.5:c.100674A>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala33558=
|
|
ENST00000591111.5:c.95751A>T
(TTN)
|
ENSP00000465570.1:p.Ala31917=
|
|
ENST00000615779.4:c.95751A>T
(TTN)
|
ENSP00000483597.1:p.Ala31917=
|
|
NM_001256850.1:c.95751A>T
(TTN)
|
NP_001243779.1:p.Ala31917=
|
|
NM_001267550.2:c.100674A>T
(TTN)
MANE Select
|
NP_001254479.2:p.Ala33558=
|
|
NM_003319.4:c.73479A>T
(TTN)
|
NP_003310.4:p.Ala24493=
|
|
NM_133378.4:c.92970A>T
(TTN)
|
NP_596869.4:p.Ala30990=
|
|
NM_133432.3:c.73854A>T
(TTN)
|
NP_597676.3:p.Ala24618=
|
|
NM_133437.4:c.74055A>T
(TTN)
|
NP_597681.4:p.Ala24685=
|
|
NR_038271.1:n.446+12437T>A
(TTN-AS1)
|
|
|
NR_038272.1:n.316+245T>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.99771A>T
(TTN)
|
XP_011510031.1:p.Ala33257=
|
|
XM_011511730.1:c.73665A>T
(TTN)
|
XP_011510032.1:p.Ala24555=
|
|
XM_011511731.1:c.73524A>T
(TTN)
|
XP_011510033.1:p.Ala24508=
|
|
XM_017004819.1:c.99567A>T
(TTN)
|
XP_016860308.1:p.Ala33189=
|
|
XM_017004820.1:c.94965A>T
(TTN)
|
XP_016860309.1:p.Ala31655=
|
|
XM_017004821.1:c.94962A>T
(TTN)
|
XP_016860310.1:p.Ala31654=
|
|
XM_017004822.1:c.92004A>T
(TTN)
|
XP_016860311.1:p.Ala30668=
|
|
XM_017004823.1:c.73620A>T
(TTN)
|
XP_016860312.1:p.Ala24540=
|
|
XM_024453094.1:c.95115A>T
(TTN)
|
XP_024308862.1:p.Ala31705=
|
|
XM_024453095.1:c.95112A>T
(TTN)
|
XP_024308863.1:p.Ala31704=
|
|
XM_024453096.1:c.94545A>T
(TTN)
|
XP_024308864.1:p.Ala31515=
|
|
XM_024453097.1:c.91887A>T
(TTN)
|
XP_024308865.1:p.Ala30629=
|
|
XM_024453098.1:c.91806A>T
(TTN)
|
XP_024308866.1:p.Ala30602=
|
|
XM_024453099.1:c.73569A>T
(TTN)
|
XP_024308867.1:p.Ala24523=
|
|
XM_024453100.1:c.63423A>T
(TTN)
|
XP_024308868.1:p.Ala21141=
|
|