ENST00000342992.11:c.86852C>G
(TTN)
|
ENSP00000343764.6:p.Thr28951Arg
|
|
ENST00000342175.11:c.67937C>G
(TTN)
|
ENSP00000340554.6:p.Thr22646Arg
|
|
ENST00000359218.10:c.67736C>G
(TTN)
|
ENSP00000352154.5:p.Thr22579Arg
|
|
ENST00000342175.10:c.67937C>G
(TTN)
|
ENSP00000340554.6:p.Thr22646Arg
|
|
ENST00000342992.10:c.86852C>G
(TTN)
|
ENSP00000343764.6:p.Thr28951Arg
|
|
ENST00000359218.9:c.67736C>G
(TTN)
|
ENSP00000352154.5:p.Thr22579Arg
|
|
ENST00000460472.6:c.67361C>G
(TTN)
|
ENSP00000434586.1:p.Thr22454Arg
|
|
ENST00000589042.5:c.94556C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr31519Arg
|
|
ENST00000591111.5:c.89633C>G
(TTN)
|
ENSP00000465570.1:p.Thr29878Arg
|
|
ENST00000615779.4:c.89633C>G
(TTN)
|
ENSP00000483597.1:p.Thr29878Arg
|
|
NM_001256850.1:c.89633C>G
(TTN)
|
NP_001243779.1:p.Thr29878Arg
|
|
NM_001267550.2:c.94556C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr31519Arg
|
|
NM_003319.4:c.67361C>G
(TTN)
|
NP_003310.4:p.Thr22454Arg
|
|
NM_133378.4:c.86852C>G
(TTN)
|
NP_596869.4:p.Thr28951Arg
|
|
NM_133432.3:c.67736C>G
(TTN)
|
NP_597676.3:p.Thr22579Arg
|
|
NM_133437.4:c.67937C>G
(TTN)
|
NP_597681.4:p.Thr22646Arg
|
|
NR_038271.1:n.446+23236G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+4511G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.93653C>G
(TTN)
|
XP_011510031.1:p.Thr31218Arg
|
|
XM_011511730.1:c.67547C>G
(TTN)
|
XP_011510032.1:p.Thr22516Arg
|
|
XM_011511731.1:c.67406C>G
(TTN)
|
XP_011510033.1:p.Thr22469Arg
|
|
XM_017004819.1:c.93449C>G
(TTN)
|
XP_016860308.1:p.Thr31150Arg
|
|
XM_017004820.1:c.88847C>G
(TTN)
|
XP_016860309.1:p.Thr29616Arg
|
|
XM_017004821.1:c.88844C>G
(TTN)
|
XP_016860310.1:p.Thr29615Arg
|
|
XM_017004822.1:c.85886C>G
(TTN)
|
XP_016860311.1:p.Thr28629Arg
|
|
XM_017004823.1:c.67502C>G
(TTN)
|
XP_016860312.1:p.Thr22501Arg
|
|
XM_024453094.1:c.88997C>G
(TTN)
|
XP_024308862.1:p.Thr29666Arg
|
|
XM_024453095.1:c.88994C>G
(TTN)
|
XP_024308863.1:p.Thr29665Arg
|
|
XM_024453096.1:c.88427C>G
(TTN)
|
XP_024308864.1:p.Thr29476Arg
|
|
XM_024453097.1:c.85769C>G
(TTN)
|
XP_024308865.1:p.Thr28590Arg
|
|
XM_024453098.1:c.85688C>G
(TTN)
|
XP_024308866.1:p.Thr28563Arg
|
|
XM_024453099.1:c.67451C>G
(TTN)
|
XP_024308867.1:p.Thr22484Arg
|
|
XM_024453100.1:c.57305C>G
(TTN)
|
XP_024308868.1:p.Thr19102Arg
|
|