ENST00000342992.11:c.85257C>T
(TTN)
|
ENSP00000343764.6:p.Asn28419=
|
|
ENST00000342175.11:c.66342C>T
(TTN)
|
ENSP00000340554.6:p.Asn22114=
|
|
ENST00000359218.10:c.66141C>T
(TTN)
|
ENSP00000352154.5:p.Asn22047=
|
|
ENST00000342175.10:c.66342C>T
(TTN)
|
ENSP00000340554.6:p.Asn22114=
|
|
ENST00000342992.10:c.85257C>T
(TTN)
|
ENSP00000343764.6:p.Asn28419=
|
|
ENST00000359218.9:c.66141C>T
(TTN)
|
ENSP00000352154.5:p.Asn22047=
|
|
ENST00000460472.6:c.65766C>T
(TTN)
|
ENSP00000434586.1:p.Asn21922=
|
|
ENST00000589042.5:c.92961C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn30987=
|
|
ENST00000591111.5:c.88038C>T
(TTN)
|
ENSP00000465570.1:p.Asn29346=
|
|
ENST00000615779.4:c.88038C>T
(TTN)
|
ENSP00000483597.1:p.Asn29346=
|
|
NM_001256850.1:c.88038C>T
(TTN)
|
NP_001243779.1:p.Asn29346=
|
|
NM_001267550.2:c.92961C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Asn30987=
|
|
NM_003319.4:c.65766C>T
(TTN)
|
NP_003310.4:p.Asn21922=
|
|
NM_133378.4:c.85257C>T
(TTN)
|
NP_596869.4:p.Asn28419=
|
|
NM_133432.3:c.66141C>T
(TTN)
|
NP_597676.3:p.Asn22047=
|
|
NM_133437.4:c.66342C>T
(TTN)
|
NP_597681.4:p.Asn22114=
|
|
NR_038271.1:n.447-22635G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6304G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.92058C>T
(TTN)
|
XP_011510031.1:p.Asn30686=
|
|
XM_011511730.1:c.65952C>T
(TTN)
|
XP_011510032.1:p.Asn21984=
|
|
XM_011511731.1:c.65811C>T
(TTN)
|
XP_011510033.1:p.Asn21937=
|
|
XM_017004819.1:c.91854C>T
(TTN)
|
XP_016860308.1:p.Asn30618=
|
|
XM_017004820.1:c.87252C>T
(TTN)
|
XP_016860309.1:p.Asn29084=
|
|
XM_017004821.1:c.87249C>T
(TTN)
|
XP_016860310.1:p.Asn29083=
|
|
XM_017004822.1:c.84291C>T
(TTN)
|
XP_016860311.1:p.Asn28097=
|
|
XM_017004823.1:c.65907C>T
(TTN)
|
XP_016860312.1:p.Asn21969=
|
|
XM_024453094.1:c.87402C>T
(TTN)
|
XP_024308862.1:p.Asn29134=
|
|
XM_024453095.1:c.87399C>T
(TTN)
|
XP_024308863.1:p.Asn29133=
|
|
XM_024453096.1:c.86832C>T
(TTN)
|
XP_024308864.1:p.Asn28944=
|
|
XM_024453097.1:c.84174C>T
(TTN)
|
XP_024308865.1:p.Asn28058=
|
|
XM_024453098.1:c.84093C>T
(TTN)
|
XP_024308866.1:p.Asn28031=
|
|
XM_024453099.1:c.65856C>T
(TTN)
|
XP_024308867.1:p.Asn21952=
|
|
XM_024453100.1:c.55710C>T
(TTN)
|
XP_024308868.1:p.Asn18570=
|
|