ENST00000342992.11:c.78781A>G
(TTN)
|
ENSP00000343764.6:p.Asn26261Asp
|
|
ENST00000342175.11:c.59866A>G
(TTN)
|
ENSP00000340554.6:p.Asn19956Asp
|
|
ENST00000359218.10:c.59665A>G
(TTN)
|
ENSP00000352154.5:p.Asn19889Asp
|
|
ENST00000342175.10:c.59866A>G
(TTN)
|
ENSP00000340554.6:p.Asn19956Asp
|
|
ENST00000342992.10:c.78781A>G
(TTN)
|
ENSP00000343764.6:p.Asn26261Asp
|
|
ENST00000359218.9:c.59665A>G
(TTN)
|
ENSP00000352154.5:p.Asn19889Asp
|
|
ENST00000460472.6:c.59290A>G
(TTN)
|
ENSP00000434586.1:p.Asn19764Asp
|
|
ENST00000589042.5:c.86485A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn28829Asp
|
|
ENST00000591111.5:c.81562A>G
(TTN)
|
ENSP00000465570.1:p.Asn27188Asp
|
|
ENST00000615779.4:c.81562A>G
(TTN)
|
ENSP00000483597.1:p.Asn27188Asp
|
|
NM_001256850.1:c.81562A>G
(TTN)
|
NP_001243779.1:p.Asn27188Asp
|
|
NM_001267550.2:c.86485A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asn28829Asp
|
|
NM_003319.4:c.59290A>G
(TTN)
|
NP_003310.4:p.Asn19764Asp
|
|
NM_133378.4:c.78781A>G
(TTN)
|
NP_596869.4:p.Asn26261Asp
|
|
NM_133432.3:c.59665A>G
(TTN)
|
NP_597676.3:p.Asn19889Asp
|
|
NM_133437.4:c.59866A>G
(TTN)
|
NP_597681.4:p.Asn19956Asp
|
|
NR_038271.1:n.447-11653T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+17286T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.85582A>G
(TTN)
|
XP_011510031.1:p.Asn28528Asp
|
|
XM_011511730.1:c.59476A>G
(TTN)
|
XP_011510032.1:p.Asn19826Asp
|
|
XM_011511731.1:c.59335A>G
(TTN)
|
XP_011510033.1:p.Asn19779Asp
|
|
XM_017004819.1:c.85378A>G
(TTN)
|
XP_016860308.1:p.Asn28460Asp
|
|
XM_017004820.1:c.80776A>G
(TTN)
|
XP_016860309.1:p.Asn26926Asp
|
|
XM_017004821.1:c.80773A>G
(TTN)
|
XP_016860310.1:p.Asn26925Asp
|
|
XM_017004822.1:c.77815A>G
(TTN)
|
XP_016860311.1:p.Asn25939Asp
|
|
XM_017004823.1:c.59431A>G
(TTN)
|
XP_016860312.1:p.Asn19811Asp
|
|
XM_024453094.1:c.80926A>G
(TTN)
|
XP_024308862.1:p.Asn26976Asp
|
|
XM_024453095.1:c.80923A>G
(TTN)
|
XP_024308863.1:p.Asn26975Asp
|
|
XM_024453096.1:c.80356A>G
(TTN)
|
XP_024308864.1:p.Asn26786Asp
|
|
XM_024453097.1:c.77698A>G
(TTN)
|
XP_024308865.1:p.Asn25900Asp
|
|
XM_024453098.1:c.77617A>G
(TTN)
|
XP_024308866.1:p.Asn25873Asp
|
|
XM_024453099.1:c.59380A>G
(TTN)
|
XP_024308867.1:p.Asn19794Asp
|
|
XM_024453100.1:c.49234A>G
(TTN)
|
XP_024308868.1:p.Asn16412Asp
|
|