ENST00000478003.2:n.1978A>G
|
|
|
ENST00000682276.1:n.1595A>G
|
|
|
ENST00000682892.1:c.1697A>G
|
ENSP00000507214.1:p.Gln566Arg
|
|
ENST00000682952.1:n.1789A>G
|
|
|
ENST00000684455.1:c.1363A>G
|
|
|
ENST00000684642.1:c.1547A>G
|
ENSP00000507355.1:p.Gln516Arg
|
|
ENST00000684740.1:n.2328A>G
|
|
|
ENST00000303236.9:c.2150A>G
MANE Select
|
ENSP00000307235.3:p.Gln717Arg
|
|
ENST00000652099.1:c.2344A>G
|
|
|
ENST00000652736.1:n.2026A>G
|
|
|
ENST00000303236.7:c.2150A>G
|
ENSP00000307235.3:p.Gln717Arg
|
|
ENST00000415570.1:c.1787A>G
|
ENSP00000412076.1:p.Gln596Arg
|
|
ENST00000419748.5:c.1697A>G
|
ENSP00000408325.1:p.Gln566Arg
|
|
ENST00000470706.1:n.48+28A>G
|
|
|
NM_001313915.1:c.1697A>G
|
NP_001300844.1:p.Gln566Arg
|
|
NM_004836.5:c.2150A>G
|
NP_004827.4:p.Gln717Arg
|
|
NM_004836.6:c.2150A>G
|
NP_004827.4:p.Gln717Arg
|
|
NR_110236.1:n.1470T>C
|
|
|
XM_005264649.3:c.1466A>G
|
XP_005264706.1:p.Gln489Arg
|
|
XR_939749.1:n.2429A>G
|
|
|
XM_017005376.2:c.1466A>G
|
XP_016860865.1:p.Gln489Arg
|
|
NM_004836.7:c.2150A>G
MANE Select
|
NP_004827.4:p.Gln717Arg
|
|
NM_001313915.2:c.1697A>G
|
NP_001300844.1:p.Gln566Arg
|
|