ENST00000342992.11:c.83350G>A
(TTN)
|
ENSP00000343764.6:p.Gly27784Ser
|
|
ENST00000342175.11:c.64435G>A
(TTN)
|
ENSP00000340554.6:p.Gly21479Ser
|
|
ENST00000359218.10:c.64234G>A
(TTN)
|
ENSP00000352154.5:p.Gly21412Ser
|
|
ENST00000342175.10:c.64435G>A
(TTN)
|
ENSP00000340554.6:p.Gly21479Ser
|
|
ENST00000342992.10:c.83350G>A
(TTN)
|
ENSP00000343764.6:p.Gly27784Ser
|
|
ENST00000359218.9:c.64234G>A
(TTN)
|
ENSP00000352154.5:p.Gly21412Ser
|
|
ENST00000460472.6:c.63859G>A
(TTN)
|
ENSP00000434586.1:p.Gly21287Ser
|
|
ENST00000589042.5:c.91054G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly30352Ser
|
|
ENST00000591111.5:c.86131G>A
(TTN)
|
ENSP00000465570.1:p.Gly28711Ser
|
|
ENST00000615779.4:c.86131G>A
(TTN)
|
ENSP00000483597.1:p.Gly28711Ser
|
|
NM_001256850.1:c.86131G>A
(TTN)
|
NP_001243779.1:p.Gly28711Ser
|
|
NM_001267550.2:c.91054G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Gly30352Ser
|
|
NM_003319.4:c.63859G>A
(TTN)
|
NP_003310.4:p.Gly21287Ser
|
|
NM_133378.4:c.83350G>A
(TTN)
|
NP_596869.4:p.Gly27784Ser
|
|
NM_133432.3:c.64234G>A
(TTN)
|
NP_597676.3:p.Gly21412Ser
|
|
NM_133437.4:c.64435G>A
(TTN)
|
NP_597681.4:p.Gly21479Ser
|
|
NR_038271.1:n.447-19454C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9485C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.90151G>A
(TTN)
|
XP_011510031.1:p.Gly30051Ser
|
|
XM_011511730.1:c.64045G>A
(TTN)
|
XP_011510032.1:p.Gly21349Ser
|
|
XM_011511731.1:c.63904G>A
(TTN)
|
XP_011510033.1:p.Gly21302Ser
|
|
XM_017004819.1:c.89947G>A
(TTN)
|
XP_016860308.1:p.Gly29983Ser
|
|
XM_017004820.1:c.85345G>A
(TTN)
|
XP_016860309.1:p.Gly28449Ser
|
|
XM_017004821.1:c.85342G>A
(TTN)
|
XP_016860310.1:p.Gly28448Ser
|
|
XM_017004822.1:c.82384G>A
(TTN)
|
XP_016860311.1:p.Gly27462Ser
|
|
XM_017004823.1:c.64000G>A
(TTN)
|
XP_016860312.1:p.Gly21334Ser
|
|
XM_024453094.1:c.85495G>A
(TTN)
|
XP_024308862.1:p.Gly28499Ser
|
|
XM_024453095.1:c.85492G>A
(TTN)
|
XP_024308863.1:p.Gly28498Ser
|
|
XM_024453096.1:c.84925G>A
(TTN)
|
XP_024308864.1:p.Gly28309Ser
|
|
XM_024453097.1:c.82267G>A
(TTN)
|
XP_024308865.1:p.Gly27423Ser
|
|
XM_024453098.1:c.82186G>A
(TTN)
|
XP_024308866.1:p.Gly27396Ser
|
|
XM_024453099.1:c.63949G>A
(TTN)
|
XP_024308867.1:p.Gly21317Ser
|
|
XM_024453100.1:c.53803G>A
(TTN)
|
XP_024308868.1:p.Gly17935Ser
|
|