ENST00000342992.11:c.67977A>C
(TTN)
|
ENSP00000343764.6:p.Lys22659Asn
|
|
ENST00000342175.11:c.49062A>C
(TTN)
|
ENSP00000340554.6:p.Lys16354Asn
|
|
ENST00000359218.10:c.48861A>C
(TTN)
|
ENSP00000352154.5:p.Lys16287Asn
|
|
ENST00000342175.10:c.49062A>C
(TTN)
|
ENSP00000340554.6:p.Lys16354Asn
|
|
ENST00000342992.10:c.67977A>C
(TTN)
|
ENSP00000343764.6:p.Lys22659Asn
|
|
ENST00000359218.9:c.48861A>C
(TTN)
|
ENSP00000352154.5:p.Lys16287Asn
|
|
ENST00000460472.6:c.48486A>C
(TTN)
|
ENSP00000434586.1:p.Lys16162Asn
|
|
ENST00000589042.5:c.75681A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Lys25227Asn
|
|
ENST00000591111.5:c.70758A>C
(TTN)
|
ENSP00000465570.1:p.Lys23586Asn
|
|
ENST00000615779.4:c.70758A>C
(TTN)
|
ENSP00000483597.1:p.Lys23586Asn
|
|
NM_001256850.1:c.70758A>C
(TTN)
|
NP_001243779.1:p.Lys23586Asn
|
|
NM_001267550.2:c.75681A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Lys25227Asn
|
|
NM_003319.4:c.48486A>C
(TTN)
|
NP_003310.4:p.Lys16162Asn
|
|
NM_133378.4:c.67977A>C
(TTN)
|
NP_596869.4:p.Lys22659Asn
|
|
NM_133432.3:c.48861A>C
(TTN)
|
NP_597676.3:p.Lys16287Asn
|
|
NM_133437.4:c.49062A>C
(TTN)
|
NP_597681.4:p.Lys16354Asn
|
|
NR_038271.1:n.447-849T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12121T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.74778A>C
(TTN)
|
XP_011510031.1:p.Lys24926Asn
|
|
XM_011511730.1:c.48672A>C
(TTN)
|
XP_011510032.1:p.Lys16224Asn
|
|
XM_011511731.1:c.48531A>C
(TTN)
|
XP_011510033.1:p.Lys16177Asn
|
|
XM_017004819.1:c.74574A>C
(TTN)
|
XP_016860308.1:p.Lys24858Asn
|
|
XM_017004820.1:c.69972A>C
(TTN)
|
XP_016860309.1:p.Lys23324Asn
|
|
XM_017004821.1:c.69969A>C
(TTN)
|
XP_016860310.1:p.Lys23323Asn
|
|
XM_017004822.1:c.67011A>C
(TTN)
|
XP_016860311.1:p.Lys22337Asn
|
|
XM_017004823.1:c.48627A>C
(TTN)
|
XP_016860312.1:p.Lys16209Asn
|
|
XM_024453094.1:c.70122A>C
(TTN)
|
XP_024308862.1:p.Lys23374Asn
|
|
XM_024453095.1:c.70119A>C
(TTN)
|
XP_024308863.1:p.Lys23373Asn
|
|
XM_024453096.1:c.69552A>C
(TTN)
|
XP_024308864.1:p.Lys23184Asn
|
|
XM_024453097.1:c.66894A>C
(TTN)
|
XP_024308865.1:p.Lys22298Asn
|
|
XM_024453098.1:c.66813A>C
(TTN)
|
XP_024308866.1:p.Lys22271Asn
|
|
XM_024453099.1:c.48576A>C
(TTN)
|
XP_024308867.1:p.Lys16192Asn
|
|
XM_024453100.1:c.38430A>C
(TTN)
|
XP_024308868.1:p.Lys12810Asn
|
|