ENST00000342992.11:c.98283T>C
(TTN)
|
ENSP00000343764.6:p.Asn32761=
|
|
ENST00000342175.11:c.79368T>C
(TTN)
|
ENSP00000340554.6:p.Asn26456=
|
|
ENST00000359218.10:c.79167T>C
(TTN)
|
ENSP00000352154.5:p.Asn26389=
|
|
ENST00000342175.10:c.79368T>C
(TTN)
|
ENSP00000340554.6:p.Asn26456=
|
|
ENST00000342992.10:c.98283T>C
(TTN)
|
ENSP00000343764.6:p.Asn32761=
|
|
ENST00000359218.9:c.79167T>C
(TTN)
|
ENSP00000352154.5:p.Asn26389=
|
|
ENST00000460472.6:c.78792T>C
(TTN)
|
ENSP00000434586.1:p.Asn26264=
|
|
ENST00000589042.5:c.105987T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Asn35329=
|
|
ENST00000591111.5:c.101064T>C
(TTN)
|
ENSP00000465570.1:p.Asn33688=
|
|
ENST00000615779.4:c.101064T>C
(TTN)
|
ENSP00000483597.1:p.Asn33688=
|
|
NM_001256850.1:c.101064T>C
(TTN)
|
NP_001243779.1:p.Asn33688=
|
|
NM_001267550.2:c.105987T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Asn35329=
|
|
NM_003319.4:c.78792T>C
(TTN)
|
NP_003310.4:p.Asn26264=
|
|
NM_133378.4:c.98283T>C
(TTN)
|
NP_596869.4:p.Asn32761=
|
|
NM_133432.3:c.79167T>C
(TTN)
|
NP_597676.3:p.Asn26389=
|
|
NM_133437.4:c.79368T>C
(TTN)
|
NP_597681.4:p.Asn26456=
|
|
NR_038271.1:n.446+6992A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5104A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.105084T>C
(TTN)
|
XP_011510031.1:p.Asn35028=
|
|
XM_011511730.1:c.78978T>C
(TTN)
|
XP_011510032.1:p.Asn26326=
|
|
XM_011511731.1:c.78837T>C
(TTN)
|
XP_011510033.1:p.Asn26279=
|
|
XM_017004819.1:c.104880T>C
(TTN)
|
XP_016860308.1:p.Asn34960=
|
|
XM_017004820.1:c.100278T>C
(TTN)
|
XP_016860309.1:p.Asn33426=
|
|
XM_017004821.1:c.100275T>C
(TTN)
|
XP_016860310.1:p.Asn33425=
|
|
XM_017004822.1:c.97317T>C
(TTN)
|
XP_016860311.1:p.Asn32439=
|
|
XM_017004823.1:c.78933T>C
(TTN)
|
XP_016860312.1:p.Asn26311=
|
|
XM_024453094.1:c.100428T>C
(TTN)
|
XP_024308862.1:p.Asn33476=
|
|
XM_024453095.1:c.100425T>C
(TTN)
|
XP_024308863.1:p.Asn33475=
|
|
XM_024453096.1:c.99858T>C
(TTN)
|
XP_024308864.1:p.Asn33286=
|
|
XM_024453097.1:c.97200T>C
(TTN)
|
XP_024308865.1:p.Asn32400=
|
|
XM_024453098.1:c.97119T>C
(TTN)
|
XP_024308866.1:p.Asn32373=
|
|
XM_024453099.1:c.78882T>C
(TTN)
|
XP_024308867.1:p.Asn26294=
|
|
XM_024453100.1:c.68736T>C
(TTN)
|
XP_024308868.1:p.Asn22912=
|
|