ENST00000342992.11:c.79939G>A
(TTN)
|
ENSP00000343764.6:p.Glu26647Lys
|
|
ENST00000342175.11:c.61024G>A
(TTN)
|
ENSP00000340554.6:p.Glu20342Lys
|
|
ENST00000359218.10:c.60823G>A
(TTN)
|
ENSP00000352154.5:p.Glu20275Lys
|
|
ENST00000342175.10:c.61024G>A
(TTN)
|
ENSP00000340554.6:p.Glu20342Lys
|
|
ENST00000342992.10:c.79939G>A
(TTN)
|
ENSP00000343764.6:p.Glu26647Lys
|
|
ENST00000359218.9:c.60823G>A
(TTN)
|
ENSP00000352154.5:p.Glu20275Lys
|
|
ENST00000460472.6:c.60448G>A
(TTN)
|
ENSP00000434586.1:p.Glu20150Lys
|
|
ENST00000589042.5:c.87643G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu29215Lys
|
|
ENST00000591111.5:c.82720G>A
(TTN)
|
ENSP00000465570.1:p.Glu27574Lys
|
|
ENST00000615779.4:c.82720G>A
(TTN)
|
ENSP00000483597.1:p.Glu27574Lys
|
|
NM_001256850.1:c.82720G>A
(TTN)
|
NP_001243779.1:p.Glu27574Lys
|
|
NM_001267550.2:c.87643G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Glu29215Lys
|
|
NM_003319.4:c.60448G>A
(TTN)
|
NP_003310.4:p.Glu20150Lys
|
|
NM_133378.4:c.79939G>A
(TTN)
|
NP_596869.4:p.Glu26647Lys
|
|
NM_133432.3:c.60823G>A
(TTN)
|
NP_597676.3:p.Glu20275Lys
|
|
NM_133437.4:c.61024G>A
(TTN)
|
NP_597681.4:p.Glu20342Lys
|
|
NR_038271.1:n.447-13589C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+15350C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.86740G>A
(TTN)
|
XP_011510031.1:p.Glu28914Lys
|
|
XM_011511730.1:c.60634G>A
(TTN)
|
XP_011510032.1:p.Glu20212Lys
|
|
XM_011511731.1:c.60493G>A
(TTN)
|
XP_011510033.1:p.Glu20165Lys
|
|
XM_017004819.1:c.86536G>A
(TTN)
|
XP_016860308.1:p.Glu28846Lys
|
|
XM_017004820.1:c.81934G>A
(TTN)
|
XP_016860309.1:p.Glu27312Lys
|
|
XM_017004821.1:c.81931G>A
(TTN)
|
XP_016860310.1:p.Glu27311Lys
|
|
XM_017004822.1:c.78973G>A
(TTN)
|
XP_016860311.1:p.Glu26325Lys
|
|
XM_017004823.1:c.60589G>A
(TTN)
|
XP_016860312.1:p.Glu20197Lys
|
|
XM_024453094.1:c.82084G>A
(TTN)
|
XP_024308862.1:p.Glu27362Lys
|
|
XM_024453095.1:c.82081G>A
(TTN)
|
XP_024308863.1:p.Glu27361Lys
|
|
XM_024453096.1:c.81514G>A
(TTN)
|
XP_024308864.1:p.Glu27172Lys
|
|
XM_024453097.1:c.78856G>A
(TTN)
|
XP_024308865.1:p.Glu26286Lys
|
|
XM_024453098.1:c.78775G>A
(TTN)
|
XP_024308866.1:p.Glu26259Lys
|
|
XM_024453099.1:c.60538G>A
(TTN)
|
XP_024308867.1:p.Glu20180Lys
|
|
XM_024453100.1:c.50392G>A
(TTN)
|
XP_024308868.1:p.Glu16798Lys
|
|