ENST00000342992.11:c.76115A>G
(TTN)
|
ENSP00000343764.6:p.Asn25372Ser
|
|
ENST00000342175.11:c.57200A>G
(TTN)
|
ENSP00000340554.6:p.Asn19067Ser
|
|
ENST00000359218.10:c.56999A>G
(TTN)
|
ENSP00000352154.5:p.Asn19000Ser
|
|
ENST00000342175.10:c.57200A>G
(TTN)
|
ENSP00000340554.6:p.Asn19067Ser
|
|
ENST00000342992.10:c.76115A>G
(TTN)
|
ENSP00000343764.6:p.Asn25372Ser
|
|
ENST00000359218.9:c.56999A>G
(TTN)
|
ENSP00000352154.5:p.Asn19000Ser
|
|
ENST00000460472.6:c.56624A>G
(TTN)
|
ENSP00000434586.1:p.Asn18875Ser
|
|
ENST00000589042.5:c.83819A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn27940Ser
|
|
ENST00000591111.5:c.78896A>G
(TTN)
|
ENSP00000465570.1:p.Asn26299Ser
|
|
ENST00000615779.4:c.78896A>G
(TTN)
|
ENSP00000483597.1:p.Asn26299Ser
|
|
NM_001256850.1:c.78896A>G
(TTN)
|
NP_001243779.1:p.Asn26299Ser
|
|
NM_001267550.2:c.83819A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Asn27940Ser
|
|
NM_003319.4:c.56624A>G
(TTN)
|
NP_003310.4:p.Asn18875Ser
|
|
NM_133378.4:c.76115A>G
(TTN)
|
NP_596869.4:p.Asn25372Ser
|
|
NM_133432.3:c.56999A>G
(TTN)
|
NP_597676.3:p.Asn19000Ser
|
|
NM_133437.4:c.57200A>G
(TTN)
|
NP_597681.4:p.Asn19067Ser
|
|
NR_038271.1:n.447-8987T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+19952T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.82916A>G
(TTN)
|
XP_011510031.1:p.Asn27639Ser
|
|
XM_011511730.1:c.56810A>G
(TTN)
|
XP_011510032.1:p.Asn18937Ser
|
|
XM_011511731.1:c.56669A>G
(TTN)
|
XP_011510033.1:p.Asn18890Ser
|
|
XM_017004819.1:c.82712A>G
(TTN)
|
XP_016860308.1:p.Asn27571Ser
|
|
XM_017004820.1:c.78110A>G
(TTN)
|
XP_016860309.1:p.Asn26037Ser
|
|
XM_017004821.1:c.78107A>G
(TTN)
|
XP_016860310.1:p.Asn26036Ser
|
|
XM_017004822.1:c.75149A>G
(TTN)
|
XP_016860311.1:p.Asn25050Ser
|
|
XM_017004823.1:c.56765A>G
(TTN)
|
XP_016860312.1:p.Asn18922Ser
|
|
XM_024453094.1:c.78260A>G
(TTN)
|
XP_024308862.1:p.Asn26087Ser
|
|
XM_024453095.1:c.78257A>G
(TTN)
|
XP_024308863.1:p.Asn26086Ser
|
|
XM_024453096.1:c.77690A>G
(TTN)
|
XP_024308864.1:p.Asn25897Ser
|
|
XM_024453097.1:c.75032A>G
(TTN)
|
XP_024308865.1:p.Asn25011Ser
|
|
XM_024453098.1:c.74951A>G
(TTN)
|
XP_024308866.1:p.Asn24984Ser
|
|
XM_024453099.1:c.56714A>G
(TTN)
|
XP_024308867.1:p.Asn18905Ser
|
|
XM_024453100.1:c.46568A>G
(TTN)
|
XP_024308868.1:p.Asn15523Ser
|
|