ENST00000342992.11:c.98281A>C
(TTN)
|
ENSP00000343764.6:p.Asn32761His
|
|
ENST00000342175.11:c.79366A>C
(TTN)
|
ENSP00000340554.6:p.Asn26456His
|
|
ENST00000359218.10:c.79165A>C
(TTN)
|
ENSP00000352154.5:p.Asn26389His
|
|
ENST00000342175.10:c.79366A>C
(TTN)
|
ENSP00000340554.6:p.Asn26456His
|
|
ENST00000342992.10:c.98281A>C
(TTN)
|
ENSP00000343764.6:p.Asn32761His
|
|
ENST00000359218.9:c.79165A>C
(TTN)
|
ENSP00000352154.5:p.Asn26389His
|
|
ENST00000460472.6:c.78790A>C
(TTN)
|
ENSP00000434586.1:p.Asn26264His
|
|
ENST00000589042.5:c.105985A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn35329His
|
|
ENST00000591111.5:c.101062A>C
(TTN)
|
ENSP00000465570.1:p.Asn33688His
|
|
ENST00000615779.4:c.101062A>C
(TTN)
|
ENSP00000483597.1:p.Asn33688His
|
|
NM_001256850.1:c.101062A>C
(TTN)
|
NP_001243779.1:p.Asn33688His
|
|
NM_001267550.2:c.105985A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn35329His
|
|
NM_003319.4:c.78790A>C
(TTN)
|
NP_003310.4:p.Asn26264His
|
|
NM_133378.4:c.98281A>C
(TTN)
|
NP_596869.4:p.Asn32761His
|
|
NM_133432.3:c.79165A>C
(TTN)
|
NP_597676.3:p.Asn26389His
|
|
NM_133437.4:c.79366A>C
(TTN)
|
NP_597681.4:p.Asn26456His
|
|
NR_038271.1:n.446+6994T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5102T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105082A>C
(TTN)
|
XP_011510031.1:p.Asn35028His
|
|
XM_011511730.1:c.78976A>C
(TTN)
|
XP_011510032.1:p.Asn26326His
|
|
XM_011511731.1:c.78835A>C
(TTN)
|
XP_011510033.1:p.Asn26279His
|
|
XM_017004819.1:c.104878A>C
(TTN)
|
XP_016860308.1:p.Asn34960His
|
|
XM_017004820.1:c.100276A>C
(TTN)
|
XP_016860309.1:p.Asn33426His
|
|
XM_017004821.1:c.100273A>C
(TTN)
|
XP_016860310.1:p.Asn33425His
|
|
XM_017004822.1:c.97315A>C
(TTN)
|
XP_016860311.1:p.Asn32439His
|
|
XM_017004823.1:c.78931A>C
(TTN)
|
XP_016860312.1:p.Asn26311His
|
|
XM_024453094.1:c.100426A>C
(TTN)
|
XP_024308862.1:p.Asn33476His
|
|
XM_024453095.1:c.100423A>C
(TTN)
|
XP_024308863.1:p.Asn33475His
|
|
XM_024453096.1:c.99856A>C
(TTN)
|
XP_024308864.1:p.Asn33286His
|
|
XM_024453097.1:c.97198A>C
(TTN)
|
XP_024308865.1:p.Asn32400His
|
|
XM_024453098.1:c.97117A>C
(TTN)
|
XP_024308866.1:p.Asn32373His
|
|
XM_024453099.1:c.78880A>C
(TTN)
|
XP_024308867.1:p.Asn26294His
|
|
XM_024453100.1:c.68734A>C
(TTN)
|
XP_024308868.1:p.Asn22912His
|
|