ENST00000493477.2:n.1490C>A
|
|
|
ENST00000682162.1:c.1016C>A
|
ENSP00000508203.1:n.1016C>A
|
|
ENST00000682567.1:n.1064C>A
|
|
|
ENST00000683521.1:c.987C>A
|
ENSP00000506864.1:p.Asn329Lys
|
|
ENST00000684161.1:n.2202C>A
|
|
|
ENST00000684483.1:c.*383C>A
|
ENSP00000507894.1:n.*383C>A
|
|
ENST00000366560.4:c.987C>A
MANE Select
|
ENSP00000355518.4:p.Asn329Lys
|
|
ENST00000366560.3:c.987C>A
|
ENSP00000355518.3:p.Asn329Lys
|
|
NM_000143.3:c.987C>A , LRG_504t1:c.987C>A
|
NP_000134.2:p.Asn329Lys
|
|
XM_011544132.1:c.759C>A
|
XP_011542434.1:p.Asn253Lys
|
|
XM_011544132.2:c.759C>A
|
XP_011542434.1:p.Asn253Lys
|
|
NM_000143.4:c.987C>A
MANE Select
|
NP_000134.2:p.Asn329Lys
|
|