ENST00000342992.11:c.92870C>A
(TTN)
|
ENSP00000343764.6:p.Pro30957His
|
|
ENST00000342175.11:c.73955C>A
(TTN)
|
ENSP00000340554.6:p.Pro24652His
|
|
ENST00000359218.10:c.73754C>A
(TTN)
|
ENSP00000352154.5:p.Pro24585His
|
|
ENST00000342175.10:c.73955C>A
(TTN)
|
ENSP00000340554.6:p.Pro24652His
|
|
ENST00000342992.10:c.92870C>A
(TTN)
|
ENSP00000343764.6:p.Pro30957His
|
|
ENST00000359218.9:c.73754C>A
(TTN)
|
ENSP00000352154.5:p.Pro24585His
|
|
ENST00000460472.6:c.73379C>A
(TTN)
|
ENSP00000434586.1:p.Pro24460His
|
|
ENST00000589042.5:c.100574C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro33525His
|
|
ENST00000591111.5:c.95651C>A
(TTN)
|
ENSP00000465570.1:p.Pro31884His
|
|
ENST00000615779.4:c.95651C>A
(TTN)
|
ENSP00000483597.1:p.Pro31884His
|
|
NM_001256850.1:c.95651C>A
(TTN)
|
NP_001243779.1:p.Pro31884His
|
|
NM_001267550.2:c.100574C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro33525His
|
|
NM_003319.4:c.73379C>A
(TTN)
|
NP_003310.4:p.Pro24460His
|
|
NM_133378.4:c.92870C>A
(TTN)
|
NP_596869.4:p.Pro30957His
|
|
NM_133432.3:c.73754C>A
(TTN)
|
NP_597676.3:p.Pro24585His
|
|
NM_133437.4:c.73955C>A
(TTN)
|
NP_597681.4:p.Pro24652His
|
|
NR_038271.1:n.446+12537G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.316+345G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.99671C>A
(TTN)
|
XP_011510031.1:p.Pro33224His
|
|
XM_011511730.1:c.73565C>A
(TTN)
|
XP_011510032.1:p.Pro24522His
|
|
XM_011511731.1:c.73424C>A
(TTN)
|
XP_011510033.1:p.Pro24475His
|
|
XM_017004819.1:c.99467C>A
(TTN)
|
XP_016860308.1:p.Pro33156His
|
|
XM_017004820.1:c.94865C>A
(TTN)
|
XP_016860309.1:p.Pro31622His
|
|
XM_017004821.1:c.94862C>A
(TTN)
|
XP_016860310.1:p.Pro31621His
|
|
XM_017004822.1:c.91904C>A
(TTN)
|
XP_016860311.1:p.Pro30635His
|
|
XM_017004823.1:c.73520C>A
(TTN)
|
XP_016860312.1:p.Pro24507His
|
|
XM_024453094.1:c.95015C>A
(TTN)
|
XP_024308862.1:p.Pro31672His
|
|
XM_024453095.1:c.95012C>A
(TTN)
|
XP_024308863.1:p.Pro31671His
|
|
XM_024453096.1:c.94445C>A
(TTN)
|
XP_024308864.1:p.Pro31482His
|
|
XM_024453097.1:c.91787C>A
(TTN)
|
XP_024308865.1:p.Pro30596His
|
|
XM_024453098.1:c.91706C>A
(TTN)
|
XP_024308866.1:p.Pro30569His
|
|
XM_024453099.1:c.73469C>A
(TTN)
|
XP_024308867.1:p.Pro24490His
|
|
XM_024453100.1:c.63323C>A
(TTN)
|
XP_024308868.1:p.Pro21108His
|
|