ENST00000292427.10:c.1165G>C
(CYP11B1)
MANE Select
|
ENSP00000292427.5:p.Asp389His
|
|
ENST00000292427.8:c.1165G>C
(CYP11B1)
|
ENSP00000292427.4:p.Asp389His
|
|
ENST00000314111.4:n.1560G>C
(CYP11B1)
|
|
|
ENST00000377675.3:c.1378G>C
(CYP11B1)
|
ENSP00000366903.3:p.Asp460His
|
|
ENST00000517471.5:c.1165G>C
(CYP11B1)
|
ENSP00000428043.1:p.Asp389His
|
|
ENST00000519285.5:c.199G>C
(CYP11B1)
|
ENSP00000430144.1:p.Asp67His
|
|
ENST00000522728.5:c.181+34044C>G
(GML)
|
ENSP00000430799.1:n.181+34044C>G
|
|
NM_000497.3:c.1165G>C
(CYP11B1)
|
NP_000488.3:p.Asp389His
|
|
NM_001026213.1:c.1165G>C
(CYP11B1)
|
NP_001021384.1:p.Asp389His
|
|
XM_011516870.1:c.1312G>C
(CYP11B1)
|
XP_011515172.1:p.Asp438His
|
|
XM_011516871.1:c.1243G>C
(CYP11B1)
|
XP_011515173.1:p.Asp415His
|
|
XM_011516872.1:c.1234G>C
(CYP11B1)
|
XP_011515174.1:p.Asp412His
|
|
XM_011516873.1:c.1312G>C
(CYP11B1)
|
XP_011515175.1:p.Asp438His
|
|
XM_011516874.1:c.1243G>C
(CYP11B1)
|
XP_011515176.1:p.Asp415His
|
|
XM_011516875.1:c.1051G>C
(CYP11B1)
|
XP_011515177.1:p.Asp351His
|
|
XM_011516876.1:c.1312G>C
(CYP11B1)
|
XP_011515178.1:p.Asp438His
|
|
XM_011516970.1:c.214+34044C>G
(GML)
|
XP_011515272.1:n.214+34044C>G
|
|
NM_000497.4:c.1165G>C
(CYP11B1)
MANE Select
|
NP_000488.3:p.Asp389His
|
|