ENST00000610179.7:c.1039G>A
MANE Select
|
ENSP00000477429.2:p.Asp347Asn
|
|
ENST00000316562.9:c.1369G>A
|
ENSP00000313377.4:p.Asp457Asn
|
|
ENST00000336066.8:c.*380G>A
|
ENSP00000477229.2:n.*380G>A
|
|
ENST00000610179.6:c.1039G>A
|
ENSP00000477429.2:p.Asp347Asn
|
|
ENST00000643504.2:c.*669G>A
|
ENSP00000495157.2:n.*669G>A
|
|
ENST00000646394.1:c.866G>A
|
|
|
ENST00000316562.8:c.1369G>A
|
ENSP00000313377.4:p.Asp457Asn
|
|
ENST00000336066.7:c.*380G>A
|
ENSP00000477229.1:n.*380G>A
|
|
ENST00000464452.1:n.604G>A
|
|
|
ENST00000495692.5:c.61G>A
|
ENSP00000476745.1:p.Asp21Asn
|
|
ENST00000497424.5:c.496G>A
|
ENSP00000417609.1:p.Asp166Asn
|
|
ENST00000610179.5:c.1000G>A
|
ENSP00000477429.1:p.Asp334Asn
|
|
ENST00000621507.1:c.496G>A
|
ENSP00000481523.1:p.Asp166Asn
|
|
NM_024960.4:c.496G>A
|
NP_079236.3:p.Asp166Asn
|
|
NM_153638.2:c.1369G>A
|
NP_705902.2:p.Asp457Asn
|
|
NM_153640.2:c.496G>A
|
NP_705904.1:p.Asp166Asn
|
|
XM_005260835.2:c.754G>A
|
XP_005260892.1:p.Asp252Asn
|
|
XM_005260836.3:c.496G>A
|
XP_005260893.3:p.Asp166Asn
|
|
XM_006723631.1:c.496G>A
|
XP_006723694.1:p.Asp166Asn
|
|
XM_011529364.1:c.1235+1761G>A
|
XP_011527666.1:n.1235+1761G>A
|
|
NM_001324191.1:c.496G>A
|
NP_001311120.1:p.Asp166Asn
|
|
NM_001324193.1:c.61G>A
|
NP_001311122.1:p.Asp21Asn
|
|
NM_024960.5:c.496G>A
|
NP_079236.3:p.Asp166Asn
|
|
NM_153638.3:c.1369G>A
|
NP_705902.2:p.Asp457Asn
|
|
NM_153640.3:c.496G>A
|
NP_705904.1:p.Asp166Asn
|
|
NR_136715.1:n.1393G>A
|
|
|
XM_005260835.3:c.754G>A
|
XP_005260892.1:p.Asp252Asn
|
|
XM_005260836.4:c.496G>A
|
XP_005260893.3:p.Asp166Asn
|
|
XM_011529364.3:c.1235+1761G>A
|
XP_011527666.1:n.1235+1761G>A
|
|
XM_017028077.2:c.61G>A
|
XP_016883566.1:p.Asp21Asn
|
|
XM_017028078.2:c.61G>A
|
XP_016883567.1:p.Asp21Asn
|
|
XM_017028079.2:c.61G>A
|
XP_016883568.1:p.Asp21Asn
|
|
XM_024452002.1:c.61G>A
|
XP_024307770.1:p.Asp21Asn
|
|
XR_002958533.1:n.2157G>A
|
|
|
NM_001324191.2:c.496G>A
|
NP_001311120.1:p.Asp166Asn
|
|
NM_001324193.2:c.61G>A
|
NP_001311122.1:p.Asp21Asn
|
|
NM_024960.6:c.496G>A
|
NP_079236.3:p.Asp166Asn
|
|
NR_136715.2:n.940G>A
|
|
|
NM_001386393.1:c.1039G>A
MANE Select
|
NP_001373322.1:p.Asp347Asn
|
|
NM_153638.4:c.1369G>A
|
NP_705902.2:p.Asp457Asn
|
|
NM_153640.4:c.496G>A
|
NP_705904.1:p.Asp166Asn
|
|