ENST00000342992.11:c.52994T>A
(TTN)
|
ENSP00000343764.6:p.Ile17665Asn
|
|
ENST00000342175.11:c.34079T>A
(TTN)
|
ENSP00000340554.6:p.Ile11360Asn
|
|
ENST00000359218.10:c.33878T>A
(TTN)
|
ENSP00000352154.5:p.Ile11293Asn
|
|
ENST00000342175.10:c.34079T>A
(TTN)
|
ENSP00000340554.6:p.Ile11360Asn
|
|
ENST00000342992.10:c.52994T>A
(TTN)
|
ENSP00000343764.6:p.Ile17665Asn
|
|
ENST00000359218.9:c.33878T>A
(TTN)
|
ENSP00000352154.5:p.Ile11293Asn
|
|
ENST00000460472.6:c.33503T>A
(TTN)
|
ENSP00000434586.1:p.Ile11168Asn
|
|
ENST00000589042.5:c.60698T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ile20233Asn
|
|
ENST00000591111.5:c.55775T>A
(TTN)
|
ENSP00000465570.1:p.Ile18592Asn
|
|
ENST00000615779.4:c.55775T>A
(TTN)
|
ENSP00000483597.1:p.Ile18592Asn
|
|
NM_001256850.1:c.55775T>A
(TTN)
|
NP_001243779.1:p.Ile18592Asn
|
|
NM_001267550.2:c.60698T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ile20233Asn
|
|
NM_003319.4:c.33503T>A
(TTN)
|
NP_003310.4:p.Ile11168Asn
|
|
NM_133378.4:c.52994T>A
(TTN)
|
NP_596869.4:p.Ile17665Asn
|
|
NM_133432.3:c.33878T>A
(TTN)
|
NP_597676.3:p.Ile11293Asn
|
|
NM_133437.4:c.34079T>A
(TTN)
|
NP_597681.4:p.Ile11360Asn
|
|
NR_038271.1:n.597-6569A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-112A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.59795T>A
(TTN)
|
XP_011510031.1:p.Ile19932Asn
|
|
XM_011511730.1:c.33689T>A
(TTN)
|
XP_011510032.1:p.Ile11230Asn
|
|
XM_011511731.1:c.33548T>A
(TTN)
|
XP_011510033.1:p.Ile11183Asn
|
|
XM_017004819.1:c.59591T>A
(TTN)
|
XP_016860308.1:p.Ile19864Asn
|
|
XM_017004820.1:c.54989T>A
(TTN)
|
XP_016860309.1:p.Ile18330Asn
|
|
XM_017004821.1:c.54986T>A
(TTN)
|
XP_016860310.1:p.Ile18329Asn
|
|
XM_017004822.1:c.52028T>A
(TTN)
|
XP_016860311.1:p.Ile17343Asn
|
|
XM_017004823.1:c.33644T>A
(TTN)
|
XP_016860312.1:p.Ile11215Asn
|
|
XM_024453094.1:c.55139T>A
(TTN)
|
XP_024308862.1:p.Ile18380Asn
|
|
XM_024453095.1:c.55136T>A
(TTN)
|
XP_024308863.1:p.Ile18379Asn
|
|
XM_024453096.1:c.54569T>A
(TTN)
|
XP_024308864.1:p.Ile18190Asn
|
|
XM_024453097.1:c.51911T>A
(TTN)
|
XP_024308865.1:p.Ile17304Asn
|
|
XM_024453098.1:c.51830T>A
(TTN)
|
XP_024308866.1:p.Ile17277Asn
|
|
XM_024453099.1:c.33593T>A
(TTN)
|
XP_024308867.1:p.Ile11198Asn
|
|
XM_024453100.1:c.23447T>A
(TTN)
|
XP_024308868.1:p.Ile7816Asn
|
|