ENST00000342992.11:c.82537G>A
(TTN)
|
ENSP00000343764.6:p.Gly27513Ser
|
|
ENST00000342175.11:c.63622G>A
(TTN)
|
ENSP00000340554.6:p.Gly21208Ser
|
|
ENST00000359218.10:c.63421G>A
(TTN)
|
ENSP00000352154.5:p.Gly21141Ser
|
|
ENST00000342175.10:c.63622G>A
(TTN)
|
ENSP00000340554.6:p.Gly21208Ser
|
|
ENST00000342992.10:c.82537G>A
(TTN)
|
ENSP00000343764.6:p.Gly27513Ser
|
|
ENST00000359218.9:c.63421G>A
(TTN)
|
ENSP00000352154.5:p.Gly21141Ser
|
|
ENST00000460472.6:c.63046G>A
(TTN)
|
ENSP00000434586.1:p.Gly21016Ser
|
|
ENST00000589042.5:c.90241G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30081Ser
|
|
ENST00000591111.5:c.85318G>A
(TTN)
|
ENSP00000465570.1:p.Gly28440Ser
|
|
ENST00000615779.4:c.85318G>A
(TTN)
|
ENSP00000483597.1:p.Gly28440Ser
|
|
NM_001256850.1:c.85318G>A
(TTN)
|
NP_001243779.1:p.Gly28440Ser
|
|
NM_001267550.2:c.90241G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30081Ser
|
|
NM_003319.4:c.63046G>A
(TTN)
|
NP_003310.4:p.Gly21016Ser
|
|
NM_133378.4:c.82537G>A
(TTN)
|
NP_596869.4:p.Gly27513Ser
|
|
NM_133432.3:c.63421G>A
(TTN)
|
NP_597676.3:p.Gly21141Ser
|
|
NM_133437.4:c.63622G>A
(TTN)
|
NP_597681.4:p.Gly21208Ser
|
|
NR_038271.1:n.447-18641C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10298C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.89338G>A
(TTN)
|
XP_011510031.1:p.Gly29780Ser
|
|
XM_011511730.1:c.63232G>A
(TTN)
|
XP_011510032.1:p.Gly21078Ser
|
|
XM_011511731.1:c.63091G>A
(TTN)
|
XP_011510033.1:p.Gly21031Ser
|
|
XM_017004819.1:c.89134G>A
(TTN)
|
XP_016860308.1:p.Gly29712Ser
|
|
XM_017004820.1:c.84532G>A
(TTN)
|
XP_016860309.1:p.Gly28178Ser
|
|
XM_017004821.1:c.84529G>A
(TTN)
|
XP_016860310.1:p.Gly28177Ser
|
|
XM_017004822.1:c.81571G>A
(TTN)
|
XP_016860311.1:p.Gly27191Ser
|
|
XM_017004823.1:c.63187G>A
(TTN)
|
XP_016860312.1:p.Gly21063Ser
|
|
XM_024453094.1:c.84682G>A
(TTN)
|
XP_024308862.1:p.Gly28228Ser
|
|
XM_024453095.1:c.84679G>A
(TTN)
|
XP_024308863.1:p.Gly28227Ser
|
|
XM_024453096.1:c.84112G>A
(TTN)
|
XP_024308864.1:p.Gly28038Ser
|
|
XM_024453097.1:c.81454G>A
(TTN)
|
XP_024308865.1:p.Gly27152Ser
|
|
XM_024453098.1:c.81373G>A
(TTN)
|
XP_024308866.1:p.Gly27125Ser
|
|
XM_024453099.1:c.63136G>A
(TTN)
|
XP_024308867.1:p.Gly21046Ser
|
|
XM_024453100.1:c.52990G>A
(TTN)
|
XP_024308868.1:p.Gly17664Ser
|
|