ENST00000342992.11:c.96658A>G
(TTN)
|
ENSP00000343764.6:p.Ser32220Gly
|
|
ENST00000342175.11:c.77743A>G
(TTN)
|
ENSP00000340554.6:p.Ser25915Gly
|
|
ENST00000359218.10:c.77542A>G
(TTN)
|
ENSP00000352154.5:p.Ser25848Gly
|
|
ENST00000342175.10:c.77743A>G
(TTN)
|
ENSP00000340554.6:p.Ser25915Gly
|
|
ENST00000342992.10:c.96658A>G
(TTN)
|
ENSP00000343764.6:p.Ser32220Gly
|
|
ENST00000359218.9:c.77542A>G
(TTN)
|
ENSP00000352154.5:p.Ser25848Gly
|
|
ENST00000460472.6:c.77167A>G
(TTN)
|
ENSP00000434586.1:p.Ser25723Gly
|
|
ENST00000589042.5:c.104362A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34788Gly
|
|
ENST00000591111.5:c.99439A>G
(TTN)
|
ENSP00000465570.1:p.Ser33147Gly
|
|
ENST00000615779.4:c.99439A>G
(TTN)
|
ENSP00000483597.1:p.Ser33147Gly
|
|
NM_001256850.1:c.99439A>G
(TTN)
|
NP_001243779.1:p.Ser33147Gly
|
|
NM_001267550.2:c.104362A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34788Gly
|
|
NM_003319.4:c.77167A>G
(TTN)
|
NP_003310.4:p.Ser25723Gly
|
|
NM_133378.4:c.96658A>G
(TTN)
|
NP_596869.4:p.Ser32220Gly
|
|
NM_133432.3:c.77542A>G
(TTN)
|
NP_597676.3:p.Ser25848Gly
|
|
NM_133437.4:c.77743A>G
(TTN)
|
NP_597681.4:p.Ser25915Gly
|
|
NR_038271.1:n.446+8617T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3479T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.103459A>G
(TTN)
|
XP_011510031.1:p.Ser34487Gly
|
|
XM_011511730.1:c.77353A>G
(TTN)
|
XP_011510032.1:p.Ser25785Gly
|
|
XM_011511731.1:c.77212A>G
(TTN)
|
XP_011510033.1:p.Ser25738Gly
|
|
XM_017004819.1:c.103255A>G
(TTN)
|
XP_016860308.1:p.Ser34419Gly
|
|
XM_017004820.1:c.98653A>G
(TTN)
|
XP_016860309.1:p.Ser32885Gly
|
|
XM_017004821.1:c.98650A>G
(TTN)
|
XP_016860310.1:p.Ser32884Gly
|
|
XM_017004822.1:c.95692A>G
(TTN)
|
XP_016860311.1:p.Ser31898Gly
|
|
XM_017004823.1:c.77308A>G
(TTN)
|
XP_016860312.1:p.Ser25770Gly
|
|
XM_024453094.1:c.98803A>G
(TTN)
|
XP_024308862.1:p.Ser32935Gly
|
|
XM_024453095.1:c.98800A>G
(TTN)
|
XP_024308863.1:p.Ser32934Gly
|
|
XM_024453096.1:c.98233A>G
(TTN)
|
XP_024308864.1:p.Ser32745Gly
|
|
XM_024453097.1:c.95575A>G
(TTN)
|
XP_024308865.1:p.Ser31859Gly
|
|
XM_024453098.1:c.95494A>G
(TTN)
|
XP_024308866.1:p.Ser31832Gly
|
|
XM_024453099.1:c.77257A>G
(TTN)
|
XP_024308867.1:p.Ser25753Gly
|
|
XM_024453100.1:c.67111A>G
(TTN)
|
XP_024308868.1:p.Ser22371Gly
|
|