ENST00000342992.11:c.78594C>T
(TTN)
|
ENSP00000343764.6:p.Val26198=
|
|
ENST00000342175.11:c.59679C>T
(TTN)
|
ENSP00000340554.6:p.Val19893=
|
|
ENST00000359218.10:c.59478C>T
(TTN)
|
ENSP00000352154.5:p.Val19826=
|
|
ENST00000342175.10:c.59679C>T
(TTN)
|
ENSP00000340554.6:p.Val19893=
|
|
ENST00000342992.10:c.78594C>T
(TTN)
|
ENSP00000343764.6:p.Val26198=
|
|
ENST00000359218.9:c.59478C>T
(TTN)
|
ENSP00000352154.5:p.Val19826=
|
|
ENST00000460472.6:c.59103C>T
(TTN)
|
ENSP00000434586.1:p.Val19701=
|
|
ENST00000589042.5:c.86298C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val28766=
|
|
ENST00000591111.5:c.81375C>T
(TTN)
|
ENSP00000465570.1:p.Val27125=
|
|
ENST00000615779.4:c.81375C>T
(TTN)
|
ENSP00000483597.1:p.Val27125=
|
|
NM_001256850.1:c.81375C>T
(TTN)
|
NP_001243779.1:p.Val27125=
|
|
NM_001267550.2:c.86298C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Val28766=
|
|
NM_003319.4:c.59103C>T
(TTN)
|
NP_003310.4:p.Val19701=
|
|
NM_133378.4:c.78594C>T
(TTN)
|
NP_596869.4:p.Val26198=
|
|
NM_133432.3:c.59478C>T
(TTN)
|
NP_597676.3:p.Val19826=
|
|
NM_133437.4:c.59679C>T
(TTN)
|
NP_597681.4:p.Val19893=
|
|
NR_038271.1:n.447-11466G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17473G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.85395C>T
(TTN)
|
XP_011510031.1:p.Val28465=
|
|
XM_011511730.1:c.59289C>T
(TTN)
|
XP_011510032.1:p.Val19763=
|
|
XM_011511731.1:c.59148C>T
(TTN)
|
XP_011510033.1:p.Val19716=
|
|
XM_017004819.1:c.85191C>T
(TTN)
|
XP_016860308.1:p.Val28397=
|
|
XM_017004820.1:c.80589C>T
(TTN)
|
XP_016860309.1:p.Val26863=
|
|
XM_017004821.1:c.80586C>T
(TTN)
|
XP_016860310.1:p.Val26862=
|
|
XM_017004822.1:c.77628C>T
(TTN)
|
XP_016860311.1:p.Val25876=
|
|
XM_017004823.1:c.59244C>T
(TTN)
|
XP_016860312.1:p.Val19748=
|
|
XM_024453094.1:c.80739C>T
(TTN)
|
XP_024308862.1:p.Val26913=
|
|
XM_024453095.1:c.80736C>T
(TTN)
|
XP_024308863.1:p.Val26912=
|
|
XM_024453096.1:c.80169C>T
(TTN)
|
XP_024308864.1:p.Val26723=
|
|
XM_024453097.1:c.77511C>T
(TTN)
|
XP_024308865.1:p.Val25837=
|
|
XM_024453098.1:c.77430C>T
(TTN)
|
XP_024308866.1:p.Val25810=
|
|
XM_024453099.1:c.59193C>T
(TTN)
|
XP_024308867.1:p.Val19731=
|
|
XM_024453100.1:c.49047C>T
(TTN)
|
XP_024308868.1:p.Val16349=
|
|