ENST00000493477.2:n.1893+9T>A
|
|
|
ENST00000682162.1:c.1419+9T>A
|
ENSP00000508203.1:n.1419+9T>A
|
|
ENST00000682567.1:n.4790+9T>A
|
|
|
ENST00000683521.1:c.1399T>A
|
ENSP00000506864.1:p.Leu467Ile
|
|
ENST00000684161.1:n.2605+9T>A
|
|
|
ENST00000684483.1:c.*786+9T>A
|
ENSP00000507894.1:n.*786+9T>A
|
|
ENST00000366560.4:c.1390+9T>A
MANE Select
|
ENSP00000355518.4:n.1390+9T>A
|
|
ENST00000366560.3:c.1390+9T>A
|
ENSP00000355518.3:n.1390+9T>A
|
|
NM_000143.3:c.1390+9T>A , LRG_504t1:c.1390+9T>A
|
NP_000134.2:n.1390+9T>A
|
|
XM_011544132.1:c.1162+9T>A
|
XP_011542434.1:n.1162+9T>A
|
|
XM_011544132.2:c.1162+9T>A
|
XP_011542434.1:n.1162+9T>A
|
|
NM_000143.4:c.1390+9T>A
MANE Select
|
NP_000134.2:n.1390+9T>A
|
|