ENST00000292427.10:c.1475G>A
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Ser492Asn
|
|
ENST00000292427.8:c.1475G>A
(CYP11B1)
|
ENSP00000292427.4:p.Ser492Asn
|
|
ENST00000314111.4:n.1672G>A
(CYP11B1)
|
|
|
ENST00000377675.3:c.1688G>A
(CYP11B1)
|
ENSP00000366903.3:p.Ser563Asn
|
|
ENST00000517471.5:c.1277G>A
(CYP11B1)
|
ENSP00000428043.1:p.Ser426Asn
|
|
ENST00000519285.5:c.509G>A
(CYP11B1)
|
ENSP00000430144.1:p.Ser170Asn
|
|
ENST00000522728.5:c.181+33185C>T
(GML)
|
ENSP00000430799.1:n.181+33185C>T
|
|
NM_000497.3:c.1475G>A
(CYP11B1)
|
NP_000488.3:p.Ser492Asn
|
|
NM_001026213.1:c.1277G>A
(CYP11B1)
|
NP_001021384.1:p.Ser426Asn
|
|
XM_011516870.1:c.1713G>A
(CYP11B1)
|
XP_011515172.1:p.Gln571=
|
|
XM_011516871.1:c.1644G>A
(CYP11B1)
|
XP_011515173.1:p.Gln548=
|
|
XM_011516872.1:c.1635G>A
(CYP11B1)
|
XP_011515174.1:p.Gln545=
|
|
XM_011516873.1:c.1622G>A
(CYP11B1)
|
XP_011515175.1:p.Ser541Asn
|
|
XM_011516874.1:c.1553G>A
(CYP11B1)
|
XP_011515176.1:p.Ser518Asn
|
|
XM_011516875.1:c.1452G>A
(CYP11B1)
|
XP_011515177.1:p.Gln484=
|
|
XM_011516876.1:c.1424G>A
(CYP11B1)
|
XP_011515178.1:p.Ser475Asn
|
|
XM_011516970.1:c.214+33185C>T
(GML)
|
XP_011515272.1:n.214+33185C>T
|
|
NM_000497.4:c.1475G>A
(CYP11B1)
MANE Select
|
NP_000488.3:p.Ser492Asn
|
|