ENST00000323110.2:c.799+32_799+33delinsGA
(CYP11B2)
MANE Select
|
ENSP00000325822.2:n.799+32_799+33delinsGA
|
|
ENST00000522728.5:c.264+627_264+628delinsTC
(GML)
|
ENSP00000430799.1:n.264+627_264+628delinsTC
|
|
NM_000498.3:c.799+32_799+33delinsGA
(CYP11B2)
MANE Select
|
NP_000489.3:n.799+32_799+33delinsGA
|
|
XM_011516877.1:c.877+32_877+33delinsGA
(CYP11B2)
|
XP_011515179.1:n.877+32_877+33delinsGA
|
|
XM_011516878.1:c.877+32_877+33delinsGA
(CYP11B2)
|
XP_011515180.1:n.877+32_877+33delinsGA
|
|
XM_011516879.1:c.799+32_799+33delinsGA
(CYP11B2)
|
XP_011515181.1:n.799+32_799+33delinsGA
|
|
XM_011516970.1:c.297+627_297+628delinsTC
(GML)
|
XP_011515272.1:n.297+627_297+628delinsTC
|
|