ENST00000342992.11:c.68552G>C
(TTN)
|
ENSP00000343764.6:p.Arg22851Thr
|
|
ENST00000342175.11:c.49637G>C
(TTN)
|
ENSP00000340554.6:p.Arg16546Thr
|
|
ENST00000359218.10:c.49436G>C
(TTN)
|
ENSP00000352154.5:p.Arg16479Thr
|
|
ENST00000342175.10:c.49637G>C
(TTN)
|
ENSP00000340554.6:p.Arg16546Thr
|
|
ENST00000342992.10:c.68552G>C
(TTN)
|
ENSP00000343764.6:p.Arg22851Thr
|
|
ENST00000359218.9:c.49436G>C
(TTN)
|
ENSP00000352154.5:p.Arg16479Thr
|
|
ENST00000460472.6:c.49061G>C
(TTN)
|
ENSP00000434586.1:p.Arg16354Thr
|
|
ENST00000589042.5:c.76256G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Arg25419Thr
|
|
ENST00000591111.5:c.71333G>C
(TTN)
|
ENSP00000465570.1:p.Arg23778Thr
|
|
ENST00000615779.4:c.71333G>C
(TTN)
|
ENSP00000483597.1:p.Arg23778Thr
|
|
NM_001256850.1:c.71333G>C
(TTN)
|
NP_001243779.1:p.Arg23778Thr
|
|
NM_001267550.2:c.76256G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Arg25419Thr
|
|
NM_003319.4:c.49061G>C
(TTN)
|
NP_003310.4:p.Arg16354Thr
|
|
NM_133378.4:c.68552G>C
(TTN)
|
NP_596869.4:p.Arg22851Thr
|
|
NM_133432.3:c.49436G>C
(TTN)
|
NP_597676.3:p.Arg16479Thr
|
|
NM_133437.4:c.49637G>C
(TTN)
|
NP_597681.4:p.Arg16546Thr
|
|
NR_038271.1:n.447-1424C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12696C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.75353G>C
(TTN)
|
XP_011510031.1:p.Arg25118Thr
|
|
XM_011511730.1:c.49247G>C
(TTN)
|
XP_011510032.1:p.Arg16416Thr
|
|
XM_011511731.1:c.49106G>C
(TTN)
|
XP_011510033.1:p.Arg16369Thr
|
|
XM_017004819.1:c.75149G>C
(TTN)
|
XP_016860308.1:p.Arg25050Thr
|
|
XM_017004820.1:c.70547G>C
(TTN)
|
XP_016860309.1:p.Arg23516Thr
|
|
XM_017004821.1:c.70544G>C
(TTN)
|
XP_016860310.1:p.Arg23515Thr
|
|
XM_017004822.1:c.67586G>C
(TTN)
|
XP_016860311.1:p.Arg22529Thr
|
|
XM_017004823.1:c.49202G>C
(TTN)
|
XP_016860312.1:p.Arg16401Thr
|
|
XM_024453094.1:c.70697G>C
(TTN)
|
XP_024308862.1:p.Arg23566Thr
|
|
XM_024453095.1:c.70694G>C
(TTN)
|
XP_024308863.1:p.Arg23565Thr
|
|
XM_024453096.1:c.70127G>C
(TTN)
|
XP_024308864.1:p.Arg23376Thr
|
|
XM_024453097.1:c.67469G>C
(TTN)
|
XP_024308865.1:p.Arg22490Thr
|
|
XM_024453098.1:c.67388G>C
(TTN)
|
XP_024308866.1:p.Arg22463Thr
|
|
XM_024453099.1:c.49151G>C
(TTN)
|
XP_024308867.1:p.Arg16384Thr
|
|
XM_024453100.1:c.39005G>C
(TTN)
|
XP_024308868.1:p.Arg13002Thr
|
|