ENST00000342992.11:c.96769G>C
(TTN)
|
ENSP00000343764.6:p.Ala32257Pro
|
|
ENST00000342175.11:c.77854G>C
(TTN)
|
ENSP00000340554.6:p.Ala25952Pro
|
|
ENST00000359218.10:c.77653G>C
(TTN)
|
ENSP00000352154.5:p.Ala25885Pro
|
|
ENST00000342175.10:c.77854G>C
(TTN)
|
ENSP00000340554.6:p.Ala25952Pro
|
|
ENST00000342992.10:c.96769G>C
(TTN)
|
ENSP00000343764.6:p.Ala32257Pro
|
|
ENST00000359218.9:c.77653G>C
(TTN)
|
ENSP00000352154.5:p.Ala25885Pro
|
|
ENST00000460472.6:c.77278G>C
(TTN)
|
ENSP00000434586.1:p.Ala25760Pro
|
|
ENST00000589042.5:c.104473G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala34825Pro
|
|
ENST00000591111.5:c.99550G>C
(TTN)
|
ENSP00000465570.1:p.Ala33184Pro
|
|
ENST00000615779.4:c.99550G>C
(TTN)
|
ENSP00000483597.1:p.Ala33184Pro
|
|
NM_001256850.1:c.99550G>C
(TTN)
|
NP_001243779.1:p.Ala33184Pro
|
|
NM_001267550.2:c.104473G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Ala34825Pro
|
|
NM_003319.4:c.77278G>C
(TTN)
|
NP_003310.4:p.Ala25760Pro
|
|
NM_133378.4:c.96769G>C
(TTN)
|
NP_596869.4:p.Ala32257Pro
|
|
NM_133432.3:c.77653G>C
(TTN)
|
NP_597676.3:p.Ala25885Pro
|
|
NM_133437.4:c.77854G>C
(TTN)
|
NP_597681.4:p.Ala25952Pro
|
|
NR_038271.1:n.446+8506C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3590C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103570G>C
(TTN)
|
XP_011510031.1:p.Ala34524Pro
|
|
XM_011511730.1:c.77464G>C
(TTN)
|
XP_011510032.1:p.Ala25822Pro
|
|
XM_011511731.1:c.77323G>C
(TTN)
|
XP_011510033.1:p.Ala25775Pro
|
|
XM_017004819.1:c.103366G>C
(TTN)
|
XP_016860308.1:p.Ala34456Pro
|
|
XM_017004820.1:c.98764G>C
(TTN)
|
XP_016860309.1:p.Ala32922Pro
|
|
XM_017004821.1:c.98761G>C
(TTN)
|
XP_016860310.1:p.Ala32921Pro
|
|
XM_017004822.1:c.95803G>C
(TTN)
|
XP_016860311.1:p.Ala31935Pro
|
|
XM_017004823.1:c.77419G>C
(TTN)
|
XP_016860312.1:p.Ala25807Pro
|
|
XM_024453094.1:c.98914G>C
(TTN)
|
XP_024308862.1:p.Ala32972Pro
|
|
XM_024453095.1:c.98911G>C
(TTN)
|
XP_024308863.1:p.Ala32971Pro
|
|
XM_024453096.1:c.98344G>C
(TTN)
|
XP_024308864.1:p.Ala32782Pro
|
|
XM_024453097.1:c.95686G>C
(TTN)
|
XP_024308865.1:p.Ala31896Pro
|
|
XM_024453098.1:c.95605G>C
(TTN)
|
XP_024308866.1:p.Ala31869Pro
|
|
XM_024453099.1:c.77368G>C
(TTN)
|
XP_024308867.1:p.Ala25790Pro
|
|
XM_024453100.1:c.67222G>C
(TTN)
|
XP_024308868.1:p.Ala22408Pro
|
|