ENST00000342992.11:c.96703T>A
(TTN)
|
ENSP00000343764.6:p.Ser32235Thr
|
|
ENST00000342175.11:c.77788T>A
(TTN)
|
ENSP00000340554.6:p.Ser25930Thr
|
|
ENST00000359218.10:c.77587T>A
(TTN)
|
ENSP00000352154.5:p.Ser25863Thr
|
|
ENST00000342175.10:c.77788T>A
(TTN)
|
ENSP00000340554.6:p.Ser25930Thr
|
|
ENST00000342992.10:c.96703T>A
(TTN)
|
ENSP00000343764.6:p.Ser32235Thr
|
|
ENST00000359218.9:c.77587T>A
(TTN)
|
ENSP00000352154.5:p.Ser25863Thr
|
|
ENST00000460472.6:c.77212T>A
(TTN)
|
ENSP00000434586.1:p.Ser25738Thr
|
|
ENST00000589042.5:c.104407T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Ser34803Thr
|
|
ENST00000591111.5:c.99484T>A
(TTN)
|
ENSP00000465570.1:p.Ser33162Thr
|
|
ENST00000615779.4:c.99484T>A
(TTN)
|
ENSP00000483597.1:p.Ser33162Thr
|
|
NM_001256850.1:c.99484T>A
(TTN)
|
NP_001243779.1:p.Ser33162Thr
|
|
NM_001267550.2:c.104407T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Ser34803Thr
|
|
NM_003319.4:c.77212T>A
(TTN)
|
NP_003310.4:p.Ser25738Thr
|
|
NM_133378.4:c.96703T>A
(TTN)
|
NP_596869.4:p.Ser32235Thr
|
|
NM_133432.3:c.77587T>A
(TTN)
|
NP_597676.3:p.Ser25863Thr
|
|
NM_133437.4:c.77788T>A
(TTN)
|
NP_597681.4:p.Ser25930Thr
|
|
NR_038271.1:n.446+8572A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3524A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103504T>A
(TTN)
|
XP_011510031.1:p.Ser34502Thr
|
|
XM_011511730.1:c.77398T>A
(TTN)
|
XP_011510032.1:p.Ser25800Thr
|
|
XM_011511731.1:c.77257T>A
(TTN)
|
XP_011510033.1:p.Ser25753Thr
|
|
XM_017004819.1:c.103300T>A
(TTN)
|
XP_016860308.1:p.Ser34434Thr
|
|
XM_017004820.1:c.98698T>A
(TTN)
|
XP_016860309.1:p.Ser32900Thr
|
|
XM_017004821.1:c.98695T>A
(TTN)
|
XP_016860310.1:p.Ser32899Thr
|
|
XM_017004822.1:c.95737T>A
(TTN)
|
XP_016860311.1:p.Ser31913Thr
|
|
XM_017004823.1:c.77353T>A
(TTN)
|
XP_016860312.1:p.Ser25785Thr
|
|
XM_024453094.1:c.98848T>A
(TTN)
|
XP_024308862.1:p.Ser32950Thr
|
|
XM_024453095.1:c.98845T>A
(TTN)
|
XP_024308863.1:p.Ser32949Thr
|
|
XM_024453096.1:c.98278T>A
(TTN)
|
XP_024308864.1:p.Ser32760Thr
|
|
XM_024453097.1:c.95620T>A
(TTN)
|
XP_024308865.1:p.Ser31874Thr
|
|
XM_024453098.1:c.95539T>A
(TTN)
|
XP_024308866.1:p.Ser31847Thr
|
|
XM_024453099.1:c.77302T>A
(TTN)
|
XP_024308867.1:p.Ser25768Thr
|
|
XM_024453100.1:c.67156T>A
(TTN)
|
XP_024308868.1:p.Ser22386Thr
|
|