|
ENST00000325748.9:c.863G>T
(PRKRA)
MANE Select
|
ENSP00000318176.4:p.Gly288Val
|
|
|
ENST00000448279.2:c.*591G>T
(PRKRA)
|
ENSP00000388455.1:n.*591G>T
|
|
|
ENST00000457633.2:c.*367G>T
(PRKRA)
|
ENSP00000408668.2:n.*367G>T
|
|
|
ENST00000474793.6:n.1004G>T
(PRKRA)
|
|
|
|
ENST00000676505.1:c.*623G>T
(PRKRA)
|
ENSP00000504163.1:n.*623G>T
|
|
|
ENST00000676586.1:n.3000G>T
(PRKRA)
|
|
|
|
ENST00000676752.1:n.2762G>T
(PRKRA)
|
|
|
|
ENST00000676832.1:c.*684G>T
(PRKRA)
|
ENSP00000503231.1:n.*684G>T
|
|
|
ENST00000676922.1:c.*591G>T
(PRKRA)
|
ENSP00000503369.1:n.*591G>T
|
|
|
ENST00000677136.1:n.2855G>T
(PRKRA)
|
|
|
|
ENST00000677206.1:c.*655G>T
(PRKRA)
|
ENSP00000503034.1:n.*655G>T
|
|
|
ENST00000677253.1:c.*560G>T
(PRKRA)
|
ENSP00000503466.1:n.*560G>T
|
|
|
ENST00000677386.1:c.*306G>T
(PRKRA)
|
ENSP00000503003.1:n.*306G>T
|
|
|
ENST00000677460.1:c.*192G>T
(PRKRA)
|
ENSP00000504507.1:n.*192G>T
|
|
|
ENST00000677584.1:c.*701G>T
(PRKRA)
|
ENSP00000504411.1:n.*701G>T
|
|
|
ENST00000677689.1:c.608G>T
(PRKRA)
|
ENSP00000502919.1:p.Gly203Val
|
|
|
ENST00000677859.1:c.716G>T
(PRKRA)
|
|
|
|
ENST00000677981.1:c.611G>T
(PRKRA)
|
ENSP00000503536.1:p.Gly204Val
|
|
|
ENST00000678053.1:c.*623G>T
(PRKRA)
|
ENSP00000504330.1:n.*623G>T
|
|
|
ENST00000678058.1:c.607G>T
(PRKRA)
|
ENSP00000503203.1:n.607G>T
|
|
|
ENST00000678167.1:c.*417G>T
(PRKRA)
|
ENSP00000504479.1:n.*417G>T
|
|
|
ENST00000678775.1:c.524G>T
(PRKRA)
|
ENSP00000504030.1:p.Gly175Val
|
|
|
ENST00000678845.1:c.524G>T
(PRKRA)
|
ENSP00000503011.1:p.Gly175Val
|
|
|
ENST00000679037.1:c.*531G>T
(PRKRA)
|
ENSP00000504421.1:n.*531G>T
|
|
|
ENST00000679202.1:n.1950G>T
(PRKRA)
|
|
|
|
ENST00000325748.8:c.863G>T
(PRKRA)
|
ENSP00000318176.4:p.Gly288Val
|
|
|
ENST00000424699.5:c.*655G>T
(PRKRA)
|
ENSP00000408029.1:n.*655G>T
|
|
|
ENST00000432031.6:c.830G>T
(PRKRA)
|
ENSP00000393883.2:p.Gly277Val
|
|
|
ENST00000487082.5:c.788G>T
(PRKRA)
|
ENSP00000430604.1:p.Gly263Val
|
|
|
ENST00000490501.5:n.1090G>T
(PRKRA)
|
|
|
|
NM_001139517.1:c.830G>T
(PRKRA)
|
NP_001132989.1:p.Gly277Val
|
|
|
NM_001139518.1:c.788G>T
(PRKRA)
|
NP_001132990.1:p.Gly263Val
|
|
|
NM_001316362.1:c.524G>T
(PRKRA)
|
NP_001303291.1:p.Gly175Val
|
|
|
NM_003690.4:c.863G>T
(PRKRA)
|
NP_003681.1:p.Gly288Val
|
|
|
NR_110204.1:n.872-1206C>A
(CHROMR)
|
|
|
|
NR_110205.1:n.716-1206C>A
(CHROMR)
|
|
|
|
NR_110206.1:n.651-1206C>A
(CHROMR)
|
|
|
|
XM_005246921.3:c.524G>T
(PRKRA)
|
XP_005246978.1:p.Gly175Val
|
|
|
XM_011512063.1:c.608G>T
(PRKRA)
|
XP_011510365.1:p.Gly203Val
|
|
|
XM_011512064.1:c.608G>T
(PRKRA)
|
XP_011510366.1:p.Gly203Val
|
|
|
XM_011512066.1:c.524G>T
(PRKRA)
|
XP_011510368.1:p.Gly175Val
|
|
|
XM_011512063.2:c.608G>T
(PRKRA)
|
XP_011510365.1:p.Gly203Val
|
|
|
XM_011512066.2:c.524G>T
(PRKRA)
|
XP_011510368.1:p.Gly175Val
|
|
|
XM_017005159.1:c.524G>T
(PRKRA)
|
XP_016860648.1:p.Gly175Val
|
|
|
XR_001739008.2:n.904G>T
(PRKRA)
|
|
|
|
NM_003690.5:c.863G>T
(PRKRA)
MANE Select
|
NP_003681.1:p.Gly288Val
|
|
|
NM_001316362.2:c.524G>T
(PRKRA)
|
NP_001303291.1:p.Gly175Val
|
|
