ENST00000342992.11:c.81659G>C
(TTN)
|
ENSP00000343764.6:p.Gly27220Ala
|
|
ENST00000342175.11:c.62744G>C
(TTN)
|
ENSP00000340554.6:p.Gly20915Ala
|
|
ENST00000359218.10:c.62543G>C
(TTN)
|
ENSP00000352154.5:p.Gly20848Ala
|
|
ENST00000342175.10:c.62744G>C
(TTN)
|
ENSP00000340554.6:p.Gly20915Ala
|
|
ENST00000342992.10:c.81659G>C
(TTN)
|
ENSP00000343764.6:p.Gly27220Ala
|
|
ENST00000359218.9:c.62543G>C
(TTN)
|
ENSP00000352154.5:p.Gly20848Ala
|
|
ENST00000460472.6:c.62168G>C
(TTN)
|
ENSP00000434586.1:p.Gly20723Ala
|
|
ENST00000589042.5:c.89363G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly29788Ala
|
|
ENST00000591111.5:c.84440G>C
(TTN)
|
ENSP00000465570.1:p.Gly28147Ala
|
|
ENST00000615779.4:c.84440G>C
(TTN)
|
ENSP00000483597.1:p.Gly28147Ala
|
|
NM_001256850.1:c.84440G>C
(TTN)
|
NP_001243779.1:p.Gly28147Ala
|
|
NM_001267550.2:c.89363G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly29788Ala
|
|
NM_003319.4:c.62168G>C
(TTN)
|
NP_003310.4:p.Gly20723Ala
|
|
NM_133378.4:c.81659G>C
(TTN)
|
NP_596869.4:p.Gly27220Ala
|
|
NM_133432.3:c.62543G>C
(TTN)
|
NP_597676.3:p.Gly20848Ala
|
|
NM_133437.4:c.62744G>C
(TTN)
|
NP_597681.4:p.Gly20915Ala
|
|
NR_038271.1:n.447-17658C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+11281C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.88460G>C
(TTN)
|
XP_011510031.1:p.Gly29487Ala
|
|
XM_011511730.1:c.62354G>C
(TTN)
|
XP_011510032.1:p.Gly20785Ala
|
|
XM_011511731.1:c.62213G>C
(TTN)
|
XP_011510033.1:p.Gly20738Ala
|
|
XM_017004819.1:c.88256G>C
(TTN)
|
XP_016860308.1:p.Gly29419Ala
|
|
XM_017004820.1:c.83654G>C
(TTN)
|
XP_016860309.1:p.Gly27885Ala
|
|
XM_017004821.1:c.83651G>C
(TTN)
|
XP_016860310.1:p.Gly27884Ala
|
|
XM_017004822.1:c.80693G>C
(TTN)
|
XP_016860311.1:p.Gly26898Ala
|
|
XM_017004823.1:c.62309G>C
(TTN)
|
XP_016860312.1:p.Gly20770Ala
|
|
XM_024453094.1:c.83804G>C
(TTN)
|
XP_024308862.1:p.Gly27935Ala
|
|
XM_024453095.1:c.83801G>C
(TTN)
|
XP_024308863.1:p.Gly27934Ala
|
|
XM_024453096.1:c.83234G>C
(TTN)
|
XP_024308864.1:p.Gly27745Ala
|
|
XM_024453097.1:c.80576G>C
(TTN)
|
XP_024308865.1:p.Gly26859Ala
|
|
XM_024453098.1:c.80495G>C
(TTN)
|
XP_024308866.1:p.Gly26832Ala
|
|
XM_024453099.1:c.62258G>C
(TTN)
|
XP_024308867.1:p.Gly20753Ala
|
|
XM_024453100.1:c.52112G>C
(TTN)
|
XP_024308868.1:p.Gly17371Ala
|
|