ENST00000342992.11:c.94947A>G
(TTN)
|
ENSP00000343764.6:p.Glu31649=
|
|
ENST00000342175.11:c.76032A>G
(TTN)
|
ENSP00000340554.6:p.Glu25344=
|
|
ENST00000359218.10:c.75831A>G
(TTN)
|
ENSP00000352154.5:p.Glu25277=
|
|
ENST00000342175.10:c.76032A>G
(TTN)
|
ENSP00000340554.6:p.Glu25344=
|
|
ENST00000342992.10:c.94947A>G
(TTN)
|
ENSP00000343764.6:p.Glu31649=
|
|
ENST00000359218.9:c.75831A>G
(TTN)
|
ENSP00000352154.5:p.Glu25277=
|
|
ENST00000460472.6:c.75456A>G
(TTN)
|
ENSP00000434586.1:p.Glu25152=
|
|
ENST00000589042.5:c.102651A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34217=
|
|
ENST00000591111.5:c.97728A>G
(TTN)
|
ENSP00000465570.1:p.Glu32576=
|
|
ENST00000615779.4:c.97728A>G
(TTN)
|
ENSP00000483597.1:p.Glu32576=
|
|
NM_001256850.1:c.97728A>G
(TTN)
|
NP_001243779.1:p.Glu32576=
|
|
NM_001267550.2:c.102651A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34217=
|
|
NM_003319.4:c.75456A>G
(TTN)
|
NP_003310.4:p.Glu25152=
|
|
NM_133378.4:c.94947A>G
(TTN)
|
NP_596869.4:p.Glu31649=
|
|
NM_133432.3:c.75831A>G
(TTN)
|
NP_597676.3:p.Glu25277=
|
|
NM_133437.4:c.76032A>G
(TTN)
|
NP_597681.4:p.Glu25344=
|
|
NR_038271.1:n.446+10328T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-1768T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.101748A>G
(TTN)
|
XP_011510031.1:p.Glu33916=
|
|
XM_011511730.1:c.75642A>G
(TTN)
|
XP_011510032.1:p.Glu25214=
|
|
XM_011511731.1:c.75501A>G
(TTN)
|
XP_011510033.1:p.Glu25167=
|
|
XM_017004819.1:c.101544A>G
(TTN)
|
XP_016860308.1:p.Glu33848=
|
|
XM_017004820.1:c.96942A>G
(TTN)
|
XP_016860309.1:p.Glu32314=
|
|
XM_017004821.1:c.96939A>G
(TTN)
|
XP_016860310.1:p.Glu32313=
|
|
XM_017004822.1:c.93981A>G
(TTN)
|
XP_016860311.1:p.Glu31327=
|
|
XM_017004823.1:c.75597A>G
(TTN)
|
XP_016860312.1:p.Glu25199=
|
|
XM_024453094.1:c.97092A>G
(TTN)
|
XP_024308862.1:p.Glu32364=
|
|
XM_024453095.1:c.97089A>G
(TTN)
|
XP_024308863.1:p.Glu32363=
|
|
XM_024453096.1:c.96522A>G
(TTN)
|
XP_024308864.1:p.Glu32174=
|
|
XM_024453097.1:c.93864A>G
(TTN)
|
XP_024308865.1:p.Glu31288=
|
|
XM_024453098.1:c.93783A>G
(TTN)
|
XP_024308866.1:p.Glu31261=
|
|
XM_024453099.1:c.75546A>G
(TTN)
|
XP_024308867.1:p.Glu25182=
|
|
XM_024453100.1:c.65400A>G
(TTN)
|
XP_024308868.1:p.Glu21800=
|
|