ENST00000342992.11:c.96646T>A
(TTN)
|
ENSP00000343764.6:p.Ser32216Thr
|
|
ENST00000342175.11:c.77731T>A
(TTN)
|
ENSP00000340554.6:p.Ser25911Thr
|
|
ENST00000359218.10:c.77530T>A
(TTN)
|
ENSP00000352154.5:p.Ser25844Thr
|
|
ENST00000342175.10:c.77731T>A
(TTN)
|
ENSP00000340554.6:p.Ser25911Thr
|
|
ENST00000342992.10:c.96646T>A
(TTN)
|
ENSP00000343764.6:p.Ser32216Thr
|
|
ENST00000359218.9:c.77530T>A
(TTN)
|
ENSP00000352154.5:p.Ser25844Thr
|
|
ENST00000460472.6:c.77155T>A
(TTN)
|
ENSP00000434586.1:p.Ser25719Thr
|
|
ENST00000589042.5:c.104350T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34784Thr
|
|
ENST00000591111.5:c.99427T>A
(TTN)
|
ENSP00000465570.1:p.Ser33143Thr
|
|
ENST00000615779.4:c.99427T>A
(TTN)
|
ENSP00000483597.1:p.Ser33143Thr
|
|
NM_001256850.1:c.99427T>A
(TTN)
|
NP_001243779.1:p.Ser33143Thr
|
|
NM_001267550.2:c.104350T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34784Thr
|
|
NM_003319.4:c.77155T>A
(TTN)
|
NP_003310.4:p.Ser25719Thr
|
|
NM_133378.4:c.96646T>A
(TTN)
|
NP_596869.4:p.Ser32216Thr
|
|
NM_133432.3:c.77530T>A
(TTN)
|
NP_597676.3:p.Ser25844Thr
|
|
NM_133437.4:c.77731T>A
(TTN)
|
NP_597681.4:p.Ser25911Thr
|
|
NR_038271.1:n.446+8629A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3467A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103447T>A
(TTN)
|
XP_011510031.1:p.Ser34483Thr
|
|
XM_011511730.1:c.77341T>A
(TTN)
|
XP_011510032.1:p.Ser25781Thr
|
|
XM_011511731.1:c.77200T>A
(TTN)
|
XP_011510033.1:p.Ser25734Thr
|
|
XM_017004819.1:c.103243T>A
(TTN)
|
XP_016860308.1:p.Ser34415Thr
|
|
XM_017004820.1:c.98641T>A
(TTN)
|
XP_016860309.1:p.Ser32881Thr
|
|
XM_017004821.1:c.98638T>A
(TTN)
|
XP_016860310.1:p.Ser32880Thr
|
|
XM_017004822.1:c.95680T>A
(TTN)
|
XP_016860311.1:p.Ser31894Thr
|
|
XM_017004823.1:c.77296T>A
(TTN)
|
XP_016860312.1:p.Ser25766Thr
|
|
XM_024453094.1:c.98791T>A
(TTN)
|
XP_024308862.1:p.Ser32931Thr
|
|
XM_024453095.1:c.98788T>A
(TTN)
|
XP_024308863.1:p.Ser32930Thr
|
|
XM_024453096.1:c.98221T>A
(TTN)
|
XP_024308864.1:p.Ser32741Thr
|
|
XM_024453097.1:c.95563T>A
(TTN)
|
XP_024308865.1:p.Ser31855Thr
|
|
XM_024453098.1:c.95482T>A
(TTN)
|
XP_024308866.1:p.Ser31828Thr
|
|
XM_024453099.1:c.77245T>A
(TTN)
|
XP_024308867.1:p.Ser25749Thr
|
|
XM_024453100.1:c.67099T>A
(TTN)
|
XP_024308868.1:p.Ser22367Thr
|
|