ENST00000292427.10:c.*16C>A
(CYP11B1)
MANE Select
|
ENSP00000292427.5:n.*16C>A
|
|
ENST00000292427.8:c.*16C>A
(CYP11B1)
|
ENSP00000292427.4:n.*16C>A
|
|
ENST00000314111.4:n.1725C>A
(CYP11B1)
|
|
|
ENST00000377675.3:c.*16C>A
(CYP11B1)
|
ENSP00000366903.3:n.*16C>A
|
|
ENST00000517471.5:c.*16C>A
(CYP11B1)
|
ENSP00000428043.1:n.*16C>A
|
|
ENST00000519285.5:c.562C>A
(CYP11B1)
|
ENSP00000430144.1:n.562C>A
|
|
ENST00000522728.5:c.181+33132G>T
(GML)
|
ENSP00000430799.1:n.181+33132G>T
|
|
NM_000497.3:c.*16C>A
(CYP11B1)
|
NP_000488.3:n.*16C>A
|
|
NM_001026213.1:c.*16C>A
(CYP11B1)
|
NP_001021384.1:n.*16C>A
|
|
XM_011516870.1:c.1766C>A
(CYP11B1)
|
XP_011515172.1:p.Pro589Gln
|
|
XM_011516871.1:c.1697C>A
(CYP11B1)
|
XP_011515173.1:p.Pro566Gln
|
|
XM_011516872.1:c.1688C>A
(CYP11B1)
|
XP_011515174.1:p.Pro563Gln
|
|
XM_011516873.1:c.*16C>A
(CYP11B1)
|
XP_011515175.1:n.*16C>A
|
|
XM_011516874.1:c.*16C>A
(CYP11B1)
|
XP_011515176.1:n.*16C>A
|
|
XM_011516875.1:c.1505C>A
(CYP11B1)
|
XP_011515177.1:p.Pro502Gln
|
|
XM_011516876.1:c.*16C>A
(CYP11B1)
|
XP_011515178.1:n.*16C>A
|
|
XM_011516970.1:c.214+33132G>T
(GML)
|
XP_011515272.1:n.214+33132G>T
|
|
NM_000497.4:c.*16C>A
(CYP11B1)
MANE Select
|
NP_000488.3:n.*16C>A
|
|