ENST00000493477.2:n.973T>A
|
|
|
ENST00000682162.1:c.499T>A
|
ENSP00000508203.1:n.499T>A
|
|
ENST00000682567.1:n.547T>A
|
|
|
ENST00000683521.1:c.470T>A
|
ENSP00000506864.1:p.Ile157Asn
|
|
ENST00000684483.1:c.470T>A
|
ENSP00000507894.1:p.Ile157Asn
|
|
ENST00000366560.4:c.470T>A
MANE Select
|
ENSP00000355518.4:p.Ile157Asn
|
|
ENST00000366560.3:c.470T>A
|
ENSP00000355518.3:p.Ile157Asn
|
|
ENST00000497042.1:n.166T>A
|
|
|
NM_000143.3:c.470T>A , LRG_504t1:c.470T>A
|
NP_000134.2:p.Ile157Asn
|
|
XM_011544132.1:c.242T>A
|
XP_011542434.1:p.Ile81Asn
|
|
XM_011544132.2:c.242T>A
|
XP_011542434.1:p.Ile81Asn
|
|
NM_000143.4:c.470T>A
MANE Select
|
NP_000134.2:p.Ile157Asn
|
|