ENST00000323110.2:c.796_797insGGG
(CYP11B2)
MANE Select
|
ENSP00000325822.2:p.Tyr266delinsTrpAsp
|
|
ENST00000522728.5:c.264+662_264+663insCCC
(GML)
|
ENSP00000430799.1:n.264+662_264+663insCCC
|
|
NM_000498.3:c.796_797insGGG
(CYP11B2)
MANE Select
|
NP_000489.3:p.Tyr266delinsTrpAsp
|
|
XM_011516877.1:c.874_875insGGG
(CYP11B2)
|
XP_011515179.1:p.Tyr292delinsTrpAsp
|
|
XM_011516878.1:c.874_875insGGG
(CYP11B2)
|
XP_011515180.1:p.Tyr292delinsTrpAsp
|
|
XM_011516879.1:c.796_797insGGG
(CYP11B2)
|
XP_011515181.1:p.Tyr266delinsTrpAsp
|
|
XM_011516970.1:c.297+662_297+663insCCC
(GML)
|
XP_011515272.1:n.297+662_297+663insCCC
|
|