ENST00000342992.11:c.92341A>G
(TTN)
|
ENSP00000343764.6:p.Thr30781Ala
|
|
ENST00000342175.11:c.73426A>G
(TTN)
|
ENSP00000340554.6:p.Thr24476Ala
|
|
ENST00000359218.10:c.73225A>G
(TTN)
|
ENSP00000352154.5:p.Thr24409Ala
|
|
ENST00000342175.10:c.73426A>G
(TTN)
|
ENSP00000340554.6:p.Thr24476Ala
|
|
ENST00000342992.10:c.92341A>G
(TTN)
|
ENSP00000343764.6:p.Thr30781Ala
|
|
ENST00000359218.9:c.73225A>G
(TTN)
|
ENSP00000352154.5:p.Thr24409Ala
|
|
ENST00000460472.6:c.72850A>G
(TTN)
|
ENSP00000434586.1:p.Thr24284Ala
|
|
ENST00000589042.5:c.100045A>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr33349Ala
|
|
ENST00000591111.5:c.95122A>G
(TTN)
|
ENSP00000465570.1:p.Thr31708Ala
|
|
ENST00000615779.4:c.95122A>G
(TTN)
|
ENSP00000483597.1:p.Thr31708Ala
|
|
NM_001256850.1:c.95122A>G
(TTN)
|
NP_001243779.1:p.Thr31708Ala
|
|
NM_001267550.2:c.100045A>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr33349Ala
|
|
NM_003319.4:c.72850A>G
(TTN)
|
NP_003310.4:p.Thr24284Ala
|
|
NM_133378.4:c.92341A>G
(TTN)
|
NP_596869.4:p.Thr30781Ala
|
|
NM_133432.3:c.73225A>G
(TTN)
|
NP_597676.3:p.Thr24409Ala
|
|
NM_133437.4:c.73426A>G
(TTN)
|
NP_597681.4:p.Thr24476Ala
|
|
NR_038271.1:n.446+13428T>C
(TTN-AS1)
|
|
|
NR_038272.1:n.317-297T>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.99142A>G
(TTN)
|
XP_011510031.1:p.Thr33048Ala
|
|
XM_011511730.1:c.73036A>G
(TTN)
|
XP_011510032.1:p.Thr24346Ala
|
|
XM_011511731.1:c.72895A>G
(TTN)
|
XP_011510033.1:p.Thr24299Ala
|
|
XM_017004819.1:c.98938A>G
(TTN)
|
XP_016860308.1:p.Thr32980Ala
|
|
XM_017004820.1:c.94336A>G
(TTN)
|
XP_016860309.1:p.Thr31446Ala
|
|
XM_017004821.1:c.94333A>G
(TTN)
|
XP_016860310.1:p.Thr31445Ala
|
|
XM_017004822.1:c.91375A>G
(TTN)
|
XP_016860311.1:p.Thr30459Ala
|
|
XM_017004823.1:c.72991A>G
(TTN)
|
XP_016860312.1:p.Thr24331Ala
|
|
XM_024453094.1:c.94486A>G
(TTN)
|
XP_024308862.1:p.Thr31496Ala
|
|
XM_024453095.1:c.94483A>G
(TTN)
|
XP_024308863.1:p.Thr31495Ala
|
|
XM_024453096.1:c.93916A>G
(TTN)
|
XP_024308864.1:p.Thr31306Ala
|
|
XM_024453097.1:c.91258A>G
(TTN)
|
XP_024308865.1:p.Thr30420Ala
|
|
XM_024453098.1:c.91177A>G
(TTN)
|
XP_024308866.1:p.Thr30393Ala
|
|
XM_024453099.1:c.72940A>G
(TTN)
|
XP_024308867.1:p.Thr24314Ala
|
|
XM_024453100.1:c.62794A>G
(TTN)
|
XP_024308868.1:p.Thr20932Ala
|
|