ENST00000588188.7:c.974-8371A>G
(PRKAR1A)
|
ENSP00000468106.2:n.974-8371A>G
|
|
ENST00000711037.1:c.974-8371A>G
(PRKAR1A)
|
ENSP00000518555.1:n.974-8371A>G
|
|
ENST00000585981.6:c.974-8371A>G
(PRKAR1A)
|
ENSP00000467311.2:n.974-8371A>G
|
|
ENST00000592554.2:c.909T>C
(FAM20A)
MANE Select
|
ENSP00000468308.1:p.Ser303=
|
|
ENST00000226094.9:n.562T>C
(FAM20A)
|
|
|
ENST00000588188.6:c.974-8371A>G
(PRKAR1A)
|
ENSP00000468106.2:n.974-8371A>G
|
|
ENST00000590074.5:c.1065T>C
(FAM20A)
|
|
|
ENST00000590873.5:c.41+916T>C
(FAM20A)
|
ENSP00000467884.1:n.41+916T>C
|
|
ENST00000592554.1:c.909T>C
(FAM20A)
|
ENSP00000468308.1:p.Ser303=
|
|
ENST00000592847.1:n.551T>C
(FAM20A)
|
|
|
NM_001243746.1:c.495T>C
(FAM20A)
|
NP_001230675.1:p.Ser165=
|
|
NM_001276290.1:c.974-8371A>G
(PRKAR1A)
|
NP_001263219.1:n.974-8371A>G
|
|
NM_017565.3:c.909T>C
(FAM20A)
|
NP_060035.2:p.Ser303=
|
|
NR_027751.1:n.599T>C
(FAM20A)
|
|
|
XM_006721959.2:c.495T>C
(FAM20A)
|
XP_006722022.1:p.Ser165=
|
|
XM_006721960.2:c.909T>C
(FAM20A)
|
XP_006722023.1:p.Ser303=
|
|
XM_011524917.1:c.809-548T>C
(FAM20A)
|
XP_011523219.1:n.809-548T>C
|
|
XM_011524918.1:c.909T>C
(FAM20A)
|
XP_011523220.1:p.Ser303=
|
|
XM_011524919.1:c.813-548T>C
(FAM20A)
|
XP_011523221.1:n.813-548T>C
|
|
XM_011524920.1:c.813-548T>C
(FAM20A)
|
XP_011523222.1:n.813-548T>C
|
|
XM_011524921.1:c.813-548T>C
(FAM20A)
|
XP_011523223.1:n.813-548T>C
|
|
XR_429905.1:n.1033T>C
(FAM20A)
|
|
|
XR_934486.1:n.1037T>C
(FAM20A)
|
|
|
XR_934487.1:n.1037T>C
(FAM20A)
|
|
|
XR_934488.1:n.1037T>C
(FAM20A)
|
|
|
XR_934489.1:n.941-548T>C
(FAM20A)
|
|
|
XR_934490.1:n.941-548T>C
(FAM20A)
|
|
|
XM_006721959.3:c.495T>C
(FAM20A)
|
XP_006722022.1:p.Ser165=
|
|
XM_011524918.3:c.909T>C
(FAM20A)
|
XP_011523220.1:p.Ser303=
|
|
XM_017024781.2:c.909T>C
(FAM20A)
|
XP_016880270.1:p.Ser303=
|
|
XR_001752543.2:n.980T>C
(FAM20A)
|
|
|
XR_001752544.2:n.980T>C
(FAM20A)
|
|
|
XR_002958041.1:n.980T>C
(FAM20A)
|
|
|
XR_429905.2:n.976T>C
(FAM20A)
|
|
|
XR_934487.3:n.980T>C
(FAM20A)
|
|
|
NM_017565.4:c.909T>C
(FAM20A)
MANE Select
|
NP_060035.2:p.Ser303=
|
|
NM_001243746.2:c.495T>C
(FAM20A)
|
NP_001230675.1:p.Ser165=
|
|
NR_027751.2:n.599T>C
(FAM20A)
|
|
|