ENST00000342992.11:c.85267G>A
(TTN)
|
ENSP00000343764.6:p.Ala28423Thr
|
|
ENST00000342175.11:c.66352G>A
(TTN)
|
ENSP00000340554.6:p.Ala22118Thr
|
|
ENST00000359218.10:c.66151G>A
(TTN)
|
ENSP00000352154.5:p.Ala22051Thr
|
|
ENST00000342175.10:c.66352G>A
(TTN)
|
ENSP00000340554.6:p.Ala22118Thr
|
|
ENST00000342992.10:c.85267G>A
(TTN)
|
ENSP00000343764.6:p.Ala28423Thr
|
|
ENST00000359218.9:c.66151G>A
(TTN)
|
ENSP00000352154.5:p.Ala22051Thr
|
|
ENST00000460472.6:c.65776G>A
(TTN)
|
ENSP00000434586.1:p.Ala21926Thr
|
|
ENST00000589042.5:c.92971G>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ala30991Thr
|
|
ENST00000591111.5:c.88048G>A
(TTN)
|
ENSP00000465570.1:p.Ala29350Thr
|
|
ENST00000615779.4:c.88048G>A
(TTN)
|
ENSP00000483597.1:p.Ala29350Thr
|
|
NM_001256850.1:c.88048G>A
(TTN)
|
NP_001243779.1:p.Ala29350Thr
|
|
NM_001267550.2:c.92971G>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ala30991Thr
|
|
NM_003319.4:c.65776G>A
(TTN)
|
NP_003310.4:p.Ala21926Thr
|
|
NM_133378.4:c.85267G>A
(TTN)
|
NP_596869.4:p.Ala28423Thr
|
|
NM_133432.3:c.66151G>A
(TTN)
|
NP_597676.3:p.Ala22051Thr
|
|
NM_133437.4:c.66352G>A
(TTN)
|
NP_597681.4:p.Ala22118Thr
|
|
NR_038271.1:n.447-22645C>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+6294C>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.92068G>A
(TTN)
|
XP_011510031.1:p.Ala30690Thr
|
|
XM_011511730.1:c.65962G>A
(TTN)
|
XP_011510032.1:p.Ala21988Thr
|
|
XM_011511731.1:c.65821G>A
(TTN)
|
XP_011510033.1:p.Ala21941Thr
|
|
XM_017004819.1:c.91864G>A
(TTN)
|
XP_016860308.1:p.Ala30622Thr
|
|
XM_017004820.1:c.87262G>A
(TTN)
|
XP_016860309.1:p.Ala29088Thr
|
|
XM_017004821.1:c.87259G>A
(TTN)
|
XP_016860310.1:p.Ala29087Thr
|
|
XM_017004822.1:c.84301G>A
(TTN)
|
XP_016860311.1:p.Ala28101Thr
|
|
XM_017004823.1:c.65917G>A
(TTN)
|
XP_016860312.1:p.Ala21973Thr
|
|
XM_024453094.1:c.87412G>A
(TTN)
|
XP_024308862.1:p.Ala29138Thr
|
|
XM_024453095.1:c.87409G>A
(TTN)
|
XP_024308863.1:p.Ala29137Thr
|
|
XM_024453096.1:c.86842G>A
(TTN)
|
XP_024308864.1:p.Ala28948Thr
|
|
XM_024453097.1:c.84184G>A
(TTN)
|
XP_024308865.1:p.Ala28062Thr
|
|
XM_024453098.1:c.84103G>A
(TTN)
|
XP_024308866.1:p.Ala28035Thr
|
|
XM_024453099.1:c.65866G>A
(TTN)
|
XP_024308867.1:p.Ala21956Thr
|
|
XM_024453100.1:c.55720G>A
(TTN)
|
XP_024308868.1:p.Ala18574Thr
|
|