ENST00000342992.11:c.41661T>C
(TTN)
|
ENSP00000343764.6:p.Thr13887=
|
|
ENST00000342175.11:c.22746T>C
(TTN)
|
ENSP00000340554.6:p.Thr7582=
|
|
ENST00000359218.10:c.22545T>C
(TTN)
|
ENSP00000352154.5:p.Thr7515=
|
|
ENST00000342175.10:c.22746T>C
(TTN)
|
ENSP00000340554.6:p.Thr7582=
|
|
ENST00000342992.10:c.41661T>C
(TTN)
|
ENSP00000343764.6:p.Thr13887=
|
|
ENST00000359218.9:c.22545T>C
(TTN)
|
ENSP00000352154.5:p.Thr7515=
|
|
ENST00000460472.6:c.22170T>C
(TTN)
|
ENSP00000434586.1:p.Thr7390=
|
|
ENST00000589042.5:c.49365T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr16455=
|
|
ENST00000591111.5:c.44442T>C
(TTN)
|
ENSP00000465570.1:p.Thr14814=
|
|
ENST00000615779.4:c.44442T>C
(TTN)
|
ENSP00000483597.1:p.Thr14814=
|
|
NM_001256850.1:c.44442T>C
(TTN)
|
NP_001243779.1:p.Thr14814=
|
|
NM_001267550.2:c.49365T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Thr16455=
|
|
NM_003319.4:c.22170T>C
(TTN)
|
NP_003310.4:p.Thr7390=
|
|
NM_133378.4:c.41661T>C
(TTN)
|
NP_596869.4:p.Thr13887=
|
|
NM_133432.3:c.22545T>C
(TTN)
|
NP_597676.3:p.Thr7515=
|
|
NM_133437.4:c.22746T>C
(TTN)
|
NP_597681.4:p.Thr7582=
|
|
NR_038271.1:n.783-117A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.48462T>C
(TTN)
|
XP_011510031.1:p.Thr16154=
|
|
XM_011511730.1:c.22356T>C
(TTN)
|
XP_011510032.1:p.Thr7452=
|
|
XM_011511731.1:c.22215T>C
(TTN)
|
XP_011510033.1:p.Thr7405=
|
|
XM_017004819.1:c.48258T>C
(TTN)
|
XP_016860308.1:p.Thr16086=
|
|
XM_017004820.1:c.43656T>C
(TTN)
|
XP_016860309.1:p.Thr14552=
|
|
XM_017004821.1:c.43653T>C
(TTN)
|
XP_016860310.1:p.Thr14551=
|
|
XM_017004822.1:c.40695T>C
(TTN)
|
XP_016860311.1:p.Thr13565=
|
|
XM_017004823.1:c.22311T>C
(TTN)
|
XP_016860312.1:p.Thr7437=
|
|
XM_024453094.1:c.43806T>C
(TTN)
|
XP_024308862.1:p.Thr14602=
|
|
XM_024453095.1:c.43803T>C
(TTN)
|
XP_024308863.1:p.Thr14601=
|
|
XM_024453096.1:c.43236T>C
(TTN)
|
XP_024308864.1:p.Thr14412=
|
|
XM_024453097.1:c.40578T>C
(TTN)
|
XP_024308865.1:p.Thr13526=
|
|
XM_024453098.1:c.40497T>C
(TTN)
|
XP_024308866.1:p.Thr13499=
|
|
XM_024453099.1:c.22260T>C
(TTN)
|
XP_024308867.1:p.Thr7420=
|
|
XM_024453100.1:c.12114T>C
(TTN)
|
XP_024308868.1:p.Thr4038=
|
|