ENST00000342992.11:c.78593T>G
(TTN)
|
ENSP00000343764.6:p.Val26198Gly
|
|
ENST00000342175.11:c.59678T>G
(TTN)
|
ENSP00000340554.6:p.Val19893Gly
|
|
ENST00000359218.10:c.59477T>G
(TTN)
|
ENSP00000352154.5:p.Val19826Gly
|
|
ENST00000342175.10:c.59678T>G
(TTN)
|
ENSP00000340554.6:p.Val19893Gly
|
|
ENST00000342992.10:c.78593T>G
(TTN)
|
ENSP00000343764.6:p.Val26198Gly
|
|
ENST00000359218.9:c.59477T>G
(TTN)
|
ENSP00000352154.5:p.Val19826Gly
|
|
ENST00000460472.6:c.59102T>G
(TTN)
|
ENSP00000434586.1:p.Val19701Gly
|
|
ENST00000589042.5:c.86297T>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Val28766Gly
|
|
ENST00000591111.5:c.81374T>G
(TTN)
|
ENSP00000465570.1:p.Val27125Gly
|
|
ENST00000615779.4:c.81374T>G
(TTN)
|
ENSP00000483597.1:p.Val27125Gly
|
|
NM_001256850.1:c.81374T>G
(TTN)
|
NP_001243779.1:p.Val27125Gly
|
|
NM_001267550.2:c.86297T>G
(TTN)
MANE Select
|
NP_001254479.2:p.Val28766Gly
|
|
NM_003319.4:c.59102T>G
(TTN)
|
NP_003310.4:p.Val19701Gly
|
|
NM_133378.4:c.78593T>G
(TTN)
|
NP_596869.4:p.Val26198Gly
|
|
NM_133432.3:c.59477T>G
(TTN)
|
NP_597676.3:p.Val19826Gly
|
|
NM_133437.4:c.59678T>G
(TTN)
|
NP_597681.4:p.Val19893Gly
|
|
NR_038271.1:n.447-11465A>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17474A>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85394T>G
(TTN)
|
XP_011510031.1:p.Val28465Gly
|
|
XM_011511730.1:c.59288T>G
(TTN)
|
XP_011510032.1:p.Val19763Gly
|
|
XM_011511731.1:c.59147T>G
(TTN)
|
XP_011510033.1:p.Val19716Gly
|
|
XM_017004819.1:c.85190T>G
(TTN)
|
XP_016860308.1:p.Val28397Gly
|
|
XM_017004820.1:c.80588T>G
(TTN)
|
XP_016860309.1:p.Val26863Gly
|
|
XM_017004821.1:c.80585T>G
(TTN)
|
XP_016860310.1:p.Val26862Gly
|
|
XM_017004822.1:c.77627T>G
(TTN)
|
XP_016860311.1:p.Val25876Gly
|
|
XM_017004823.1:c.59243T>G
(TTN)
|
XP_016860312.1:p.Val19748Gly
|
|
XM_024453094.1:c.80738T>G
(TTN)
|
XP_024308862.1:p.Val26913Gly
|
|
XM_024453095.1:c.80735T>G
(TTN)
|
XP_024308863.1:p.Val26912Gly
|
|
XM_024453096.1:c.80168T>G
(TTN)
|
XP_024308864.1:p.Val26723Gly
|
|
XM_024453097.1:c.77510T>G
(TTN)
|
XP_024308865.1:p.Val25837Gly
|
|
XM_024453098.1:c.77429T>G
(TTN)
|
XP_024308866.1:p.Val25810Gly
|
|
XM_024453099.1:c.59192T>G
(TTN)
|
XP_024308867.1:p.Val19731Gly
|
|
XM_024453100.1:c.49046T>G
(TTN)
|
XP_024308868.1:p.Val16349Gly
|
|