|
ENST00000419558.7:c.443T>C
(GNAS)
|
ENSP00000416234.2:p.Val148Ala
|
|
|
ENST00000453292.7:c.443T>C
(GNAS)
|
ENSP00000392000.2:p.Val148Ala
|
|
|
ENST00000419558.6:c.443T>C
(GNAS)
|
ENSP00000416234.2:p.Val148Ala
|
|
|
ENST00000453292.6:c.443T>C
(GNAS)
|
ENSP00000392000.2:p.Val148Ala
|
|
|
ENST00000657090.1:c.-39+609T>C
(GNAS)
|
ENSP00000499380.1:n.-39+609T>C
|
|
|
ENST00000667293.1:c.-27-301T>C
(GNAS)
|
ENSP00000499293.1:n.-27-301T>C
|
|
|
ENST00000313949.11:c.443T>C
(GNAS)
|
ENSP00000323571.7:p.Val148Ala
|
|
|
ENST00000371075.7:c.443T>C
(GNAS)
MANE Plus Clinical
|
ENSP00000360115.3:p.Val148Ala
|
|
|
ENST00000371098.6:c.443T>C
(GNAS)
|
ENSP00000360139.2:p.Val148Ala
|
|
|
ENST00000419558.5:c.46T>C
(GNAS)
|
|
|
|
ENST00000453292.5:c.206T>C
(GNAS)
|
ENSP00000392000.1:p.Val69Ala
|
|
|
NM_016592.2:c.443T>C
(GNAS)
|
NP_057676.1:p.Val148Ala
|
|
|
NM_016592.3:c.443T>C
(GNAS)
|
NP_057676.1:p.Val148Ala
|
|
|
NR_002785.2:n.819+1388A>G
(GNAS-AS1)
|
|
|
|
XM_017027821.1:c.443T>C
(GNAS)
|
XP_016883310.1:p.Val148Ala
|
|
|
XM_017027822.1:c.443T>C
(GNAS)
|
XP_016883311.1:p.Val148Ala
|
|
|
XM_024451872.1:c.-295T>C
(GNAS)
|
XP_024307640.1:n.-295T>C
|
|
|
NM_016592.4:c.443T>C
(GNAS)
|
NP_057676.1:p.Val148Ala
|
|
|
NM_016592.5:c.443T>C
(GNAS)
MANE Plus Clinical
|
NP_057676.1:p.Val148Ala
|
|
