|
NM_004836.7:c.497A>G
MANE Select
|
NP_004827.4:p.Gln166Arg
|
|
ENST00000303236.9:c.497A>G
MANE Select
|
ENSP00000307235.3:p.Gln166Arg
|
|
NM_001313915.1:c.44A>G
|
NP_001300844.1:p.Gln15Arg
|
|
NM_001313915.2:c.44A>G
|
NP_001300844.1:p.Gln15Arg
|
|
NM_004836.5:c.497A>G
|
NP_004827.4:p.Gln166Arg
|
|
NM_004836.6:c.497A>G
|
NP_004827.4:p.Gln166Arg
|
|
ENST00000303236.7:c.497A>G
|
ENSP00000307235.3:p.Gln166Arg
|
|
ENST00000415570.1:c.134A>G
|
ENSP00000412076.1:p.Gln45Arg
|
|
ENST00000419748.5:c.44A>G
|
ENSP00000408325.1:p.Gln15Arg
|
|
ENST00000652099.1:c.495A>G
|
|
|
ENST00000652736.1:n.373A>G
|
|
|
ENST00000682892.1:c.44A>G
|
ENSP00000507214.1:p.Gln15Arg
|
|
XM_017005376.2:c.-384A>G
|
XP_016860865.1:n.-384A>G
|
|
XR_939749.1:n.706A>G
|
|