ENST00000493477.2:n.1857T>A
|
|
|
ENST00000682162.1:c.1383T>A
|
ENSP00000508203.1:n.1383T>A
|
|
ENST00000682567.1:n.4754T>A
|
|
|
ENST00000683521.1:c.1354T>A
|
ENSP00000506864.1:p.Ser452Thr
|
|
ENST00000684161.1:n.2569T>A
|
|
|
ENST00000684483.1:c.*750T>A
|
ENSP00000507894.1:n.*750T>A
|
|
ENST00000366560.4:c.1354T>A
MANE Select
|
ENSP00000355518.4:p.Ser452Thr
|
|
ENST00000366560.3:c.1354T>A
|
ENSP00000355518.3:p.Ser452Thr
|
|
NM_000143.3:c.1354T>A , LRG_504t1:c.1354T>A
|
NP_000134.2:p.Ser452Thr
|
|
XM_011544132.1:c.1126T>A
|
XP_011542434.1:p.Ser376Thr
|
|
XM_011544132.2:c.1126T>A
|
XP_011542434.1:p.Ser376Thr
|
|
NM_000143.4:c.1354T>A
MANE Select
|
NP_000134.2:p.Ser452Thr
|
|