|
ENST00000361510.8:c.1034G>A
MANE Select
|
ENSP00000355324.2:p.Arg345Gln
|
|
|
ENST00000361828.7:c.869G>A
|
ENSP00000354429.3:p.Arg290Gln
|
|
|
ENST00000361908.8:c.980G>A
|
ENSP00000354681.3:p.Arg327Gln
|
|
|
ENST00000392436.7:c.869G>A
|
ENSP00000376231.3:p.Arg290Gln
|
|
|
ENST00000392437.6:c.923G>A
|
ENSP00000376232.2:p.Arg308Gln
|
|
|
ENST00000642289.1:c.964G>A
|
|
|
|
ENST00000642445.1:c.869G>A
|
ENSP00000495535.1:p.Arg290Gln
|
|
|
ENST00000642593.1:c.869G>A
|
ENSP00000494273.1:p.Arg290Gln
|
|
|
ENST00000643329.1:c.551G>A
|
ENSP00000493673.1:p.Arg184Gln
|
|
|
ENST00000643737.1:c.*950G>A
|
ENSP00000494210.1:n.*950G>A
|
|
|
ENST00000644595.1:c.869G>A
|
ENSP00000494121.1:p.Arg290Gln
|
|
|
ENST00000644629.1:c.529G>A
|
|
|
|
ENST00000644841.1:c.497G>A
|
ENSP00000493988.1:p.Arg166Gln
|
|
|
ENST00000644959.1:c.838G>A
|
|
|
|
ENST00000645553.1:c.884G>A
|
ENSP00000494725.1:p.Arg295Gln
|
|
|
ENST00000646085.1:c.*347G>A
|
ENSP00000494509.1:n.*347G>A
|
|
|
ENST00000646277.1:c.1034G>A
|
ENSP00000495289.1:p.Arg345Gln
|
|
|
ENST00000646699.1:c.964G>A
|
|
|
|
ENST00000646793.1:c.761G>A
|
ENSP00000494512.1:p.Arg254Gln
|
|
|
ENST00000361150.6:c.872G>A
|
ENSP00000354781.2:p.Arg291Gln
|
|
|
ENST00000361510.6:c.1034G>A
|
ENSP00000355324.2:p.Arg345Gln
|
|
|
ENST00000361715.6:c.926G>A
|
ENSP00000355311.2:p.Arg309Gln
|
|
|
ENST00000361828.6:c.923G>A
|
ENSP00000354429.2:p.Arg308Gln
|
|
|
ENST00000361908.7:c.980G>A
|
ENSP00000354681.3:p.Arg327Gln
|
|
|
ENST00000392438.7:c.869G>A
|
ENSP00000376233.3:p.Arg290Gln
|
|
|
ENST00000475899.1:n.65G>A
|
|
|
|
ENST00000495476.1:n.390G>A
|
|
|
|
ENST00000497189.5:n.355G>A
|
|
|
|
NM_015560.2:c.869G>A , LRG_337t1:c.869G>A
|
NP_056375.2:p.Arg290Gln
|
|
|
NM_130831.2:c.761G>A
|
NP_570844.1:p.Arg254Gln
|
|
|
NM_130832.2:c.815G>A
|
NP_570845.1:p.Arg272Gln
|
|
|
NM_130833.2:c.872G>A
|
NP_570846.1:p.Arg291Gln
|
|
|
NM_130834.2:c.923G>A
|
NP_570847.2:p.Arg308Gln
|
|
|
NM_130835.2:c.926G>A
|
NP_570848.1:p.Arg309Gln
|
|
|
NM_130836.2:c.980G>A
|
NP_570849.2:p.Arg327Gln
|
|
|
NM_130837.2:c.1034G>A , LRG_337t2:c.1034G>A
|
NP_570850.2:p.Arg345Gln
|
|
|
XM_011512863.1:c.1034G>A
|
XP_011511165.1:p.Arg345Gln
|
|
|
XM_011512864.1:c.980G>A
|
XP_011511166.1:p.Arg327Gln
|
|
|
XM_011512865.1:c.923G>A
|
XP_011511167.1:p.Arg308Gln
|
|
|
XM_011512866.1:c.872G>A
|
XP_011511168.1:p.Arg291Gln
|
|
|
XM_011512867.1:c.869G>A
|
XP_011511169.1:p.Arg290Gln
|
|
|
XM_011512868.1:c.761G>A
|
XP_011511170.1:p.Arg254Gln
|
|
|
XM_011512869.1:c.1034G>A
|
XP_011511171.1:p.Arg345Gln
|
|
|
NM_001354663.1:c.500G>A
|
NP_001341592.1:p.Arg167Gln
|
|
|
NM_001354664.1:c.497G>A
|
NP_001341593.1:p.Arg166Gln
|
|
|
XR_001740158.2:n.1263G>A
|
|
|
|
XR_001740159.2:n.1098G>A
|
|
|
|
NM_001354663.2:c.500G>A
|
NP_001341592.1:p.Arg167Gln
|
|
|
NM_001354664.2:c.497G>A
|
NP_001341593.1:p.Arg166Gln
|
|
|
NM_130831.3:c.761G>A
|
NP_570844.1:p.Arg254Gln
|
|
|
NM_130832.3:c.815G>A
|
NP_570845.1:p.Arg272Gln
|
|
|
NM_130834.3:c.923G>A
|
NP_570847.2:p.Arg308Gln
|
|
|
NM_130836.3:c.980G>A
|
NP_570849.2:p.Arg327Gln
|
|
|
NM_015560.3:c.869G>A
|
NP_056375.2:p.Arg290Gln
|
|
|
NM_130833.3:c.872G>A
|
NP_570846.1:p.Arg291Gln
|
|
|
NM_130835.3:c.926G>A
|
NP_570848.1:p.Arg309Gln
|
|
|
NM_130837.3:c.1034G>A
MANE Select
|
NP_570850.2:p.Arg345Gln
|
|
