|
ENST00000325748.9:c.856G>T
(PRKRA)
MANE Select
|
ENSP00000318176.4:p.Gly286Cys
|
|
|
ENST00000448279.2:c.*584G>T
(PRKRA)
|
ENSP00000388455.1:n.*584G>T
|
|
|
ENST00000457633.2:c.*360G>T
(PRKRA)
|
ENSP00000408668.2:n.*360G>T
|
|
|
ENST00000474793.6:n.997G>T
(PRKRA)
|
|
|
|
ENST00000676505.1:c.*616G>T
(PRKRA)
|
ENSP00000504163.1:n.*616G>T
|
|
|
ENST00000676586.1:n.2993G>T
(PRKRA)
|
|
|
|
ENST00000676752.1:n.2755G>T
(PRKRA)
|
|
|
|
ENST00000676832.1:c.*677G>T
(PRKRA)
|
ENSP00000503231.1:n.*677G>T
|
|
|
ENST00000676922.1:c.*584G>T
(PRKRA)
|
ENSP00000503369.1:n.*584G>T
|
|
|
ENST00000677136.1:n.2848G>T
(PRKRA)
|
|
|
|
ENST00000677206.1:c.*648G>T
(PRKRA)
|
ENSP00000503034.1:n.*648G>T
|
|
|
ENST00000677253.1:c.*553G>T
(PRKRA)
|
ENSP00000503466.1:n.*553G>T
|
|
|
ENST00000677386.1:c.*299G>T
(PRKRA)
|
ENSP00000503003.1:n.*299G>T
|
|
|
ENST00000677460.1:c.*185G>T
(PRKRA)
|
ENSP00000504507.1:n.*185G>T
|
|
|
ENST00000677584.1:c.*694G>T
(PRKRA)
|
ENSP00000504411.1:n.*694G>T
|
|
|
ENST00000677689.1:c.601G>T
(PRKRA)
|
ENSP00000502919.1:p.Gly201Cys
|
|
|
ENST00000677859.1:c.709G>T
(PRKRA)
|
|
|
|
ENST00000677981.1:c.604G>T
(PRKRA)
|
ENSP00000503536.1:p.Gly202Cys
|
|
|
ENST00000678053.1:c.*616G>T
(PRKRA)
|
ENSP00000504330.1:n.*616G>T
|
|
|
ENST00000678058.1:c.600G>T
(PRKRA)
|
ENSP00000503203.1:n.600G>T
|
|
|
ENST00000678167.1:c.*410G>T
(PRKRA)
|
ENSP00000504479.1:n.*410G>T
|
|
|
ENST00000678775.1:c.517G>T
(PRKRA)
|
ENSP00000504030.1:p.Gly173Cys
|
|
|
ENST00000678845.1:c.517G>T
(PRKRA)
|
ENSP00000503011.1:p.Gly173Cys
|
|
|
ENST00000679037.1:c.*524G>T
(PRKRA)
|
ENSP00000504421.1:n.*524G>T
|
|
|
ENST00000679202.1:n.1943G>T
(PRKRA)
|
|
|
|
ENST00000325748.8:c.856G>T
(PRKRA)
|
ENSP00000318176.4:p.Gly286Cys
|
|
|
ENST00000424699.5:c.*648G>T
(PRKRA)
|
ENSP00000408029.1:n.*648G>T
|
|
|
ENST00000432031.6:c.823G>T
(PRKRA)
|
ENSP00000393883.2:p.Gly275Cys
|
|
|
ENST00000487082.5:c.781G>T
(PRKRA)
|
ENSP00000430604.1:p.Gly261Cys
|
|
|
ENST00000490501.5:n.1083G>T
(PRKRA)
|
|
|
|
NM_001139517.1:c.823G>T
(PRKRA)
|
NP_001132989.1:p.Gly275Cys
|
|
|
NM_001139518.1:c.781G>T
(PRKRA)
|
NP_001132990.1:p.Gly261Cys
|
|
|
NM_001316362.1:c.517G>T
(PRKRA)
|
NP_001303291.1:p.Gly173Cys
|
|
|
NM_003690.4:c.856G>T
(PRKRA)
|
NP_003681.1:p.Gly286Cys
|
|
|
NR_110204.1:n.872-1199C>A
(CHROMR)
|
|
|
|
NR_110205.1:n.716-1199C>A
(CHROMR)
|
|
|
|
NR_110206.1:n.651-1199C>A
(CHROMR)
|
|
|
|
XM_005246921.3:c.517G>T
(PRKRA)
|
XP_005246978.1:p.Gly173Cys
|
|
|
XM_011512063.1:c.601G>T
(PRKRA)
|
XP_011510365.1:p.Gly201Cys
|
|
|
XM_011512064.1:c.601G>T
(PRKRA)
|
XP_011510366.1:p.Gly201Cys
|
|
|
XM_011512066.1:c.517G>T
(PRKRA)
|
XP_011510368.1:p.Gly173Cys
|
|
|
XM_011512063.2:c.601G>T
(PRKRA)
|
XP_011510365.1:p.Gly201Cys
|
|
|
XM_011512066.2:c.517G>T
(PRKRA)
|
XP_011510368.1:p.Gly173Cys
|
|
|
XM_017005159.1:c.517G>T
(PRKRA)
|
XP_016860648.1:p.Gly173Cys
|
|
|
XR_001739008.2:n.897G>T
(PRKRA)
|
|
|
|
NM_003690.5:c.856G>T
(PRKRA)
MANE Select
|
NP_003681.1:p.Gly286Cys
|
|
|
NM_001316362.2:c.517G>T
(PRKRA)
|
NP_001303291.1:p.Gly173Cys
|
|
