|
ENST00000419558.7:c.*42+97G>T
(GNAS)
|
ENSP00000416234.2:n.*42+97G>T
|
|
|
ENST00000453292.7:c.780+97G>T
(GNAS)
|
ENSP00000392000.2:n.780+97G>T
|
|
|
ENST00000306090.12:c.43+97G>T
(GNAS)
|
ENSP00000304472.12:n.43+97G>T
|
|
|
ENST00000419558.6:c.*42+97G>T
(GNAS)
|
ENSP00000416234.2:n.*42+97G>T
|
|
|
ENST00000453292.6:c.*42+97G>T
(GNAS)
|
ENSP00000392000.2:n.*42+97G>T
|
|
|
ENST00000657090.1:c.-39+1043G>T
(GNAS)
|
ENSP00000499380.1:n.-39+1043G>T
|
|
|
ENST00000667293.1:c.10+97G>T
(GNAS)
|
ENSP00000499293.1:n.10+97G>T
|
|
|
ENST00000313949.11:c.*42+97G>T
(GNAS)
|
ENSP00000323571.7:n.*42+97G>T
|
|
|
ENST00000371075.7:c.*42+97G>T
(GNAS)
MANE Plus Clinical
|
ENSP00000360115.3:n.*42+97G>T
|
|
|
ENST00000371098.6:c.*42+97G>T
(GNAS)
|
ENSP00000360139.2:n.*42+97G>T
|
|
|
ENST00000419558.5:c.383+97G>T
(GNAS)
|
|
|
|
ENST00000453292.5:c.543+97G>T
(GNAS)
|
ENSP00000392000.1:n.543+97G>T
|
|
|
NM_016592.2:c.*42+97G>T
(GNAS)
|
NP_057676.1:n.*42+97G>T
|
|
|
NM_016592.3:c.*42+97G>T
(GNAS)
|
NP_057676.1:n.*42+97G>T
|
|
|
NR_002785.2:n.819+954C>A
(GNAS-AS1)
|
|
|
|
XM_017027815.1:c.43+97G>T
(GNAS)
|
XP_016883304.1:n.43+97G>T
|
|
|
XM_017027821.1:c.*42+97G>T
(GNAS)
|
XP_016883310.1:n.*42+97G>T
|
|
|
XM_017027822.1:c.*42+97G>T
(GNAS)
|
XP_016883311.1:n.*42+97G>T
|
|
|
XM_024451872.1:c.43+97G>T
(GNAS)
|
XP_024307640.1:n.43+97G>T
|
|
|
NM_016592.4:c.*42+97G>T
(GNAS)
|
NP_057676.1:n.*42+97G>T
|
|
|
NM_016592.5:c.*42+97G>T
(GNAS)
MANE Plus Clinical
|
NP_057676.1:n.*42+97G>T
|
|
