ENST00000642493.1:c.*488G>A
|
ENSP00000493524.1:n.*488G>A
|
|
ENST00000642498.1:c.848G>A
|
ENSP00000493631.1:p.Arg283His
|
|
ENST00000642538.1:c.*192G>A
|
ENSP00000493927.1:n.*192G>A
|
|
ENST00000643188.1:c.848G>A
|
ENSP00000493903.1:p.Arg283His
|
|
ENST00000643443.1:c.*555G>A
|
ENSP00000495572.1:n.*555G>A
|
|
ENST00000643502.1:c.505G>A
|
|
|
ENST00000643908.1:n.1066G>A
|
|
|
ENST00000644538.1:n.1125G>A
|
|
|
ENST00000644793.1:c.848G>A
|
ENSP00000495750.1:p.Arg283His
|
|
ENST00000645328.1:c.226G>A
|
|
|
ENST00000645408.1:c.381G>A
|
|
|
ENST00000645723.1:n.2087G>A
|
|
|
ENST00000646405.1:c.*266G>A
|
ENSP00000493744.1:n.*266G>A
|
|
ENST00000646497.1:n.793G>A
|
|
|
ENST00000646512.1:n.994G>A
|
|
|
ENST00000646735.1:c.515G>A
|
ENSP00000493763.1:p.Arg172His
|
|
ENST00000651619.1:c.848G>A
MANE Select
|
ENSP00000498303.1:p.Arg283His
|
|
ENST00000216951.6:c.848G>A
|
ENSP00000216951.2:p.Arg283His
|
|
ENST00000451957.2:c.515G>A
|
ENSP00000407517.2:p.Arg172His
|
|
NM_000178.2:c.848G>A
|
NP_000169.1:p.Arg283His
|
|
XM_005260406.3:c.848G>A
|
XP_005260463.1:p.Arg283His
|
|
XM_011528796.1:c.848G>A
|
XP_011527098.1:p.Arg283His
|
|
NM_000178.4:c.848G>A
MANE Select
|
NP_000169.1:p.Arg283His
|
|
NM_001322494.1:c.848G>A
|
NP_001309423.1:p.Arg283His
|
|
NM_001322495.1:c.848G>A
|
NP_001309424.1:p.Arg283His
|
|