ENST00000268314.9:c.998A>G
MANE Select
|
ENSP00000268314.4:p.Gln333Arg
|
|
ENST00000268314.8:c.998A>G
|
ENSP00000268314.4:p.Gln333Arg
|
|
ENST00000408912.7:c.1283A>G
|
ENSP00000386125.3:p.Gln428Arg
|
|
ENST00000457010.6:c.998A>G
|
ENSP00000399561.2:p.Gln333Arg
|
|
ENST00000538189.5:c.506A>G
|
ENSP00000443995.2:p.Gln169Arg
|
|
ENST00000563544.5:c.998A>G
|
ENSP00000456877.1:p.Gln333Arg
|
|
ENST00000564900.1:c.213-227A>G
|
|
|
NM_001105247.1:c.998A>G
|
NP_001098717.1:p.Gln333Arg
|
|
NM_001288767.1:c.1283A>G
|
NP_001275696.1:p.Gln428Arg
|
|
NM_001301820.1:c.1094A>G
|
NP_001288749.1:p.Gln365Arg
|
|
NM_024742.2:c.998A>G
|
NP_079018.1:p.Gln333Arg
|
|
XM_006721091.1:c.1094A>G
|
XP_006721154.1:p.Gln365Arg
|
|
XM_006721091.3:c.1094A>G
|
XP_006721154.1:p.Gln365Arg
|
|
XM_024450448.1:c.1094A>G
|
XP_024306216.1:p.Gln365Arg
|
|
XM_024450449.1:c.1094A>G
|
XP_024306217.1:p.Gln365Arg
|
|
NM_001105247.2:c.998A>G
MANE Select
|
NP_001098717.1:p.Gln333Arg
|
|
NM_001288767.2:c.1283A>G
|
NP_001275696.1:p.Gln428Arg
|
|