ENST00000478003.2:n.2301A>G
|
|
|
ENST00000682103.1:c.14A>G
|
|
|
ENST00000682276.1:n.1918A>G
|
|
|
ENST00000682892.1:c.2020A>G
|
ENSP00000507214.1:p.Asn674Asp
|
|
ENST00000682952.1:n.2112A>G
|
|
|
ENST00000684455.1:c.1686A>G
|
|
|
ENST00000684642.1:c.1870A>G
|
ENSP00000507355.1:p.Asn624Asp
|
|
ENST00000684740.1:n.2651A>G
|
|
|
ENST00000303236.9:c.2473A>G
MANE Select
|
ENSP00000307235.3:p.Asn825Asp
|
|
ENST00000652099.1:c.2667A>G
|
|
|
ENST00000652736.1:n.2349A>G
|
|
|
ENST00000303236.7:c.2473A>G
|
ENSP00000307235.3:p.Asn825Asp
|
|
ENST00000415570.1:c.2110A>G
|
ENSP00000412076.1:p.Asn704Asp
|
|
ENST00000419748.5:c.2020A>G
|
ENSP00000408325.1:p.Asn674Asp
|
|
ENST00000470706.1:n.116A>G
|
|
|
NM_001313915.1:c.2020A>G
|
NP_001300844.1:p.Asn674Asp
|
|
NM_004836.5:c.2473A>G
|
NP_004827.4:p.Asn825Asp
|
|
NM_004836.6:c.2473A>G
|
NP_004827.4:p.Asn825Asp
|
|
NR_110236.1:n.1147T>C
|
|
|
XM_005264649.3:c.1789A>G
|
XP_005264706.1:p.Asn597Asp
|
|
XM_017005376.2:c.1789A>G
|
XP_016860865.1:p.Asn597Asp
|
|
NM_004836.7:c.2473A>G
MANE Select
|
NP_004827.4:p.Asn825Asp
|
|
NM_001313915.2:c.2020A>G
|
NP_001300844.1:p.Asn674Asp
|
|