ENST00000342992.11:c.60827C>A
(TTN)
|
ENSP00000343764.6:p.Pro20276His
|
|
ENST00000342175.11:c.41912C>A
(TTN)
|
ENSP00000340554.6:p.Pro13971His
|
|
ENST00000359218.10:c.41711C>A
(TTN)
|
ENSP00000352154.5:p.Pro13904His
|
|
ENST00000342175.10:c.41912C>A
(TTN)
|
ENSP00000340554.6:p.Pro13971His
|
|
ENST00000342992.10:c.60827C>A
(TTN)
|
ENSP00000343764.6:p.Pro20276His
|
|
ENST00000359218.9:c.41711C>A
(TTN)
|
ENSP00000352154.5:p.Pro13904His
|
|
ENST00000460472.6:c.41336C>A
(TTN)
|
ENSP00000434586.1:p.Pro13779His
|
|
ENST00000589042.5:c.68531C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro22844His
|
|
ENST00000591111.5:c.63608C>A
(TTN)
|
ENSP00000465570.1:p.Pro21203His
|
|
ENST00000615779.4:c.63608C>A
(TTN)
|
ENSP00000483597.1:p.Pro21203His
|
|
NM_001256850.1:c.63608C>A
(TTN)
|
NP_001243779.1:p.Pro21203His
|
|
NM_001267550.2:c.68531C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro22844His
|
|
NM_003319.4:c.41336C>A
(TTN)
|
NP_003310.4:p.Pro13779His
|
|
NM_133378.4:c.60827C>A
(TTN)
|
NP_596869.4:p.Pro20276His
|
|
NM_133432.3:c.41711C>A
(TTN)
|
NP_597676.3:p.Pro13904His
|
|
NM_133437.4:c.41912C>A
(TTN)
|
NP_597681.4:p.Pro13971His
|
|
NR_038271.1:n.596+6446G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-4677G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.67628C>A
(TTN)
|
XP_011510031.1:p.Pro22543His
|
|
XM_011511730.1:c.41522C>A
(TTN)
|
XP_011510032.1:p.Pro13841His
|
|
XM_011511731.1:c.41381C>A
(TTN)
|
XP_011510033.1:p.Pro13794His
|
|
XM_017004819.1:c.67424C>A
(TTN)
|
XP_016860308.1:p.Pro22475His
|
|
XM_017004820.1:c.62822C>A
(TTN)
|
XP_016860309.1:p.Pro20941His
|
|
XM_017004821.1:c.62819C>A
(TTN)
|
XP_016860310.1:p.Pro20940His
|
|
XM_017004822.1:c.59861C>A
(TTN)
|
XP_016860311.1:p.Pro19954His
|
|
XM_017004823.1:c.41477C>A
(TTN)
|
XP_016860312.1:p.Pro13826His
|
|
XM_024453094.1:c.62972C>A
(TTN)
|
XP_024308862.1:p.Pro20991His
|
|
XM_024453095.1:c.62969C>A
(TTN)
|
XP_024308863.1:p.Pro20990His
|
|
XM_024453096.1:c.62402C>A
(TTN)
|
XP_024308864.1:p.Pro20801His
|
|
XM_024453097.1:c.59744C>A
(TTN)
|
XP_024308865.1:p.Pro19915His
|
|
XM_024453098.1:c.59663C>A
(TTN)
|
XP_024308866.1:p.Pro19888His
|
|
XM_024453099.1:c.41426C>A
(TTN)
|
XP_024308867.1:p.Pro13809His
|
|
XM_024453100.1:c.31280C>A
(TTN)
|
XP_024308868.1:p.Pro10427His
|
|