ENST00000367027.5:c.744G>C
(HSD11B1)
MANE Select
|
ENSP00000355994.3:p.Gly248=
|
|
ENST00000261465.5:c.744G>C
(HSD11B1)
|
ENSP00000261465.2:p.Gly248=
|
|
ENST00000367027.4:c.744G>C
(HSD11B1)
|
ENSP00000355994.3:p.Gly248=
|
|
ENST00000367028.6:c.744G>C
(HSD11B1)
|
ENSP00000355995.1:p.Gly248=
|
|
NM_001206741.1:c.744G>C
(HSD11B1)
|
NP_001193670.1:p.Gly248=
|
|
NM_005525.3:c.744G>C
(HSD11B1)
|
NP_005516.1:p.Gly248=
|
|
NM_181755.2:c.744G>C
(HSD11B1)
|
NP_861420.1:p.Gly248=
|
|
XR_922542.1:n.3119+8111C>G
(HSD11B1-AS1)
|
|
|
XR_922543.1:n.3110+8111C>G
(HSD11B1-AS1)
|
|
|
XR_922547.1:n.3090+8111C>G
(HSD11B1-AS1)
|
|
|
XR_922549.1:n.124+23090C>G
(HSD11B1-AS1)
|
|
|
NR_134510.1:n.66+8111C>G
(HSD11B1-AS1)
|
|
|
NM_005525.4:c.744G>C
(HSD11B1)
MANE Select
|
NP_005516.1:p.Gly248=
|
|
NM_001206741.2:c.744G>C
(HSD11B1)
|
NP_001193670.1:p.Gly248=
|
|
NM_181755.3:c.744G>C
(HSD11B1)
|
NP_861420.1:p.Gly248=
|
|