ENST00000342992.11:c.96691T>A
(TTN)
|
ENSP00000343764.6:p.Ser32231Thr
|
|
ENST00000342175.11:c.77776T>A
(TTN)
|
ENSP00000340554.6:p.Ser25926Thr
|
|
ENST00000359218.10:c.77575T>A
(TTN)
|
ENSP00000352154.5:p.Ser25859Thr
|
|
ENST00000342175.10:c.77776T>A
(TTN)
|
ENSP00000340554.6:p.Ser25926Thr
|
|
ENST00000342992.10:c.96691T>A
(TTN)
|
ENSP00000343764.6:p.Ser32231Thr
|
|
ENST00000359218.9:c.77575T>A
(TTN)
|
ENSP00000352154.5:p.Ser25859Thr
|
|
ENST00000460472.6:c.77200T>A
(TTN)
|
ENSP00000434586.1:p.Ser25734Thr
|
|
ENST00000589042.5:c.104395T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34799Thr
|
|
ENST00000591111.5:c.99472T>A
(TTN)
|
ENSP00000465570.1:p.Ser33158Thr
|
|
ENST00000615779.4:c.99472T>A
(TTN)
|
ENSP00000483597.1:p.Ser33158Thr
|
|
NM_001256850.1:c.99472T>A
(TTN)
|
NP_001243779.1:p.Ser33158Thr
|
|
NM_001267550.2:c.104395T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34799Thr
|
|
NM_003319.4:c.77200T>A
(TTN)
|
NP_003310.4:p.Ser25734Thr
|
|
NM_133378.4:c.96691T>A
(TTN)
|
NP_596869.4:p.Ser32231Thr
|
|
NM_133432.3:c.77575T>A
(TTN)
|
NP_597676.3:p.Ser25859Thr
|
|
NM_133437.4:c.77776T>A
(TTN)
|
NP_597681.4:p.Ser25926Thr
|
|
NR_038271.1:n.446+8584A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3512A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103492T>A
(TTN)
|
XP_011510031.1:p.Ser34498Thr
|
|
XM_011511730.1:c.77386T>A
(TTN)
|
XP_011510032.1:p.Ser25796Thr
|
|
XM_011511731.1:c.77245T>A
(TTN)
|
XP_011510033.1:p.Ser25749Thr
|
|
XM_017004819.1:c.103288T>A
(TTN)
|
XP_016860308.1:p.Ser34430Thr
|
|
XM_017004820.1:c.98686T>A
(TTN)
|
XP_016860309.1:p.Ser32896Thr
|
|
XM_017004821.1:c.98683T>A
(TTN)
|
XP_016860310.1:p.Ser32895Thr
|
|
XM_017004822.1:c.95725T>A
(TTN)
|
XP_016860311.1:p.Ser31909Thr
|
|
XM_017004823.1:c.77341T>A
(TTN)
|
XP_016860312.1:p.Ser25781Thr
|
|
XM_024453094.1:c.98836T>A
(TTN)
|
XP_024308862.1:p.Ser32946Thr
|
|
XM_024453095.1:c.98833T>A
(TTN)
|
XP_024308863.1:p.Ser32945Thr
|
|
XM_024453096.1:c.98266T>A
(TTN)
|
XP_024308864.1:p.Ser32756Thr
|
|
XM_024453097.1:c.95608T>A
(TTN)
|
XP_024308865.1:p.Ser31870Thr
|
|
XM_024453098.1:c.95527T>A
(TTN)
|
XP_024308866.1:p.Ser31843Thr
|
|
XM_024453099.1:c.77290T>A
(TTN)
|
XP_024308867.1:p.Ser25764Thr
|
|
XM_024453100.1:c.67144T>A
(TTN)
|
XP_024308868.1:p.Ser22382Thr
|
|