ENST00000697149.1:c.1329A>G
|
ENSP00000513138.1:n.1329A>G
|
|
ENST00000697150.1:c.1387A>G
|
ENSP00000513139.1:n.1387A>G
|
|
ENST00000697151.1:c.1320A>G
|
ENSP00000513140.1:n.1320A>G
|
|
ENST00000697164.1:c.1400A>G
|
ENSP00000513153.1:p.His467Arg
|
|
ENST00000697165.1:c.1187A>G
|
ENSP00000513154.1:p.His396Arg
|
|
ENST00000347310.10:c.1490A>G
MANE Select
|
ENSP00000321345.5:p.His497Arg
|
|
ENST00000637002.1:c.881A>G
|
ENSP00000490340.1:p.His294Arg
|
|
ENST00000347310.9:c.1490A>G
|
ENSP00000321345.5:p.His497Arg
|
|
ENST00000395227.2:c.284A>G
|
ENSP00000378652.2:p.His95Arg
|
|
ENST00000425614.3:c.725A>G
|
ENSP00000387640.2:p.His242Arg
|
|
ENST00000473881.2:c.*316A>G
|
ENSP00000486667.1:n.*316A>G
|
|
NM_144701.2:c.1490A>G
|
NP_653302.2:p.His497Arg
|
|
XM_005270516.2:c.728A>G
|
XP_005270573.1:p.His243Arg
|
|
XM_011540789.1:c.1580A>G
|
XP_011539091.1:p.His527Arg
|
|
XM_011540790.1:c.1490A>G
|
XP_011539092.1:p.His497Arg
|
|
XM_011540791.1:c.1490A>G
|
XP_011539093.1:p.His497Arg
|
|
XM_011540790.3:c.1490A>G
|
XP_011539092.1:p.His497Arg
|
|
XM_011540791.3:c.1490A>G
|
XP_011539093.1:p.His497Arg
|
|
XR_001736993.1:n.1570A>G
|
|
|
NM_144701.3:c.1490A>G
MANE Select
|
NP_653302.2:p.His497Arg
|
|