ENST00000342992.11:c.76347A>G
(TTN)
|
ENSP00000343764.6:p.Val25449=
|
|
ENST00000342175.11:c.57432A>G
(TTN)
|
ENSP00000340554.6:p.Val19144=
|
|
ENST00000359218.10:c.57231A>G
(TTN)
|
ENSP00000352154.5:p.Val19077=
|
|
ENST00000342175.10:c.57432A>G
(TTN)
|
ENSP00000340554.6:p.Val19144=
|
|
ENST00000342992.10:c.76347A>G
(TTN)
|
ENSP00000343764.6:p.Val25449=
|
|
ENST00000359218.9:c.57231A>G
(TTN)
|
ENSP00000352154.5:p.Val19077=
|
|
ENST00000460472.6:c.56856A>G
(TTN)
|
ENSP00000434586.1:p.Val18952=
|
|
ENST00000589042.5:c.84051A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val28017=
|
|
ENST00000591111.5:c.79128A>G
(TTN)
|
ENSP00000465570.1:p.Val26376=
|
|
ENST00000615779.4:c.79128A>G
(TTN)
|
ENSP00000483597.1:p.Val26376=
|
|
NM_001256850.1:c.79128A>G
(TTN)
|
NP_001243779.1:p.Val26376=
|
|
NM_001267550.2:c.84051A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val28017=
|
|
NM_003319.4:c.56856A>G
(TTN)
|
NP_003310.4:p.Val18952=
|
|
NM_133378.4:c.76347A>G
(TTN)
|
NP_596869.4:p.Val25449=
|
|
NM_133432.3:c.57231A>G
(TTN)
|
NP_597676.3:p.Val19077=
|
|
NM_133437.4:c.57432A>G
(TTN)
|
NP_597681.4:p.Val19144=
|
|
NR_038271.1:n.447-9219T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+19720T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.83148A>G
(TTN)
|
XP_011510031.1:p.Val27716=
|
|
XM_011511730.1:c.57042A>G
(TTN)
|
XP_011510032.1:p.Val19014=
|
|
XM_011511731.1:c.56901A>G
(TTN)
|
XP_011510033.1:p.Val18967=
|
|
XM_017004819.1:c.82944A>G
(TTN)
|
XP_016860308.1:p.Val27648=
|
|
XM_017004820.1:c.78342A>G
(TTN)
|
XP_016860309.1:p.Val26114=
|
|
XM_017004821.1:c.78339A>G
(TTN)
|
XP_016860310.1:p.Val26113=
|
|
XM_017004822.1:c.75381A>G
(TTN)
|
XP_016860311.1:p.Val25127=
|
|
XM_017004823.1:c.56997A>G
(TTN)
|
XP_016860312.1:p.Val18999=
|
|
XM_024453094.1:c.78492A>G
(TTN)
|
XP_024308862.1:p.Val26164=
|
|
XM_024453095.1:c.78489A>G
(TTN)
|
XP_024308863.1:p.Val26163=
|
|
XM_024453096.1:c.77922A>G
(TTN)
|
XP_024308864.1:p.Val25974=
|
|
XM_024453097.1:c.75264A>G
(TTN)
|
XP_024308865.1:p.Val25088=
|
|
XM_024453098.1:c.75183A>G
(TTN)
|
XP_024308866.1:p.Val25061=
|
|
XM_024453099.1:c.56946A>G
(TTN)
|
XP_024308867.1:p.Val18982=
|
|
XM_024453100.1:c.46800A>G
(TTN)
|
XP_024308868.1:p.Val15600=
|
|