ENST00000610179.7:c.1048A>T
MANE Select
|
ENSP00000477429.2:p.Arg350Trp
|
|
ENST00000316562.9:c.1378A>T
|
ENSP00000313377.4:p.Arg460Trp
|
|
ENST00000336066.8:c.*389A>T
|
ENSP00000477229.2:n.*389A>T
|
|
ENST00000610179.6:c.1048A>T
|
ENSP00000477429.2:p.Arg350Trp
|
|
ENST00000643504.2:c.*678A>T
|
ENSP00000495157.2:n.*678A>T
|
|
ENST00000646394.1:c.875A>T
|
|
|
ENST00000316562.8:c.1378A>T
|
ENSP00000313377.4:p.Arg460Trp
|
|
ENST00000336066.7:c.*389A>T
|
ENSP00000477229.1:n.*389A>T
|
|
ENST00000464452.1:n.613A>T
|
|
|
ENST00000495692.5:c.70A>T
|
ENSP00000476745.1:p.Arg24Trp
|
|
ENST00000497424.5:c.505A>T
|
ENSP00000417609.1:p.Arg169Trp
|
|
ENST00000610179.5:c.1009A>T
|
ENSP00000477429.1:p.Arg337Trp
|
|
ENST00000621507.1:c.505A>T
|
ENSP00000481523.1:p.Arg169Trp
|
|
NM_024960.4:c.505A>T
|
NP_079236.3:p.Arg169Trp
|
|
NM_153638.2:c.1378A>T
|
NP_705902.2:p.Arg460Trp
|
|
NM_153640.2:c.505A>T
|
NP_705904.1:p.Arg169Trp
|
|
XM_005260835.2:c.763A>T
|
XP_005260892.1:p.Arg255Trp
|
|
XM_005260836.3:c.505A>T
|
XP_005260893.3:p.Arg169Trp
|
|
XM_006723631.1:c.505A>T
|
XP_006723694.1:p.Arg169Trp
|
|
XM_011529364.1:c.1235+1770A>T
|
XP_011527666.1:n.1235+1770A>T
|
|
NM_001324191.1:c.505A>T
|
NP_001311120.1:p.Arg169Trp
|
|
NM_001324193.1:c.70A>T
|
NP_001311122.1:p.Arg24Trp
|
|
NM_024960.5:c.505A>T
|
NP_079236.3:p.Arg169Trp
|
|
NM_153638.3:c.1378A>T
|
NP_705902.2:p.Arg460Trp
|
|
NM_153640.3:c.505A>T
|
NP_705904.1:p.Arg169Trp
|
|
NR_136715.1:n.1402A>T
|
|
|
XM_005260835.3:c.763A>T
|
XP_005260892.1:p.Arg255Trp
|
|
XM_005260836.4:c.505A>T
|
XP_005260893.3:p.Arg169Trp
|
|
XM_011529364.3:c.1235+1770A>T
|
XP_011527666.1:n.1235+1770A>T
|
|
XM_017028077.2:c.70A>T
|
XP_016883566.1:p.Arg24Trp
|
|
XM_017028078.2:c.70A>T
|
XP_016883567.1:p.Arg24Trp
|
|
XM_017028079.2:c.70A>T
|
XP_016883568.1:p.Arg24Trp
|
|
XM_024452002.1:c.70A>T
|
XP_024307770.1:p.Arg24Trp
|
|
XR_002958533.1:n.2166A>T
|
|
|
NM_001324191.2:c.505A>T
|
NP_001311120.1:p.Arg169Trp
|
|
NM_001324193.2:c.70A>T
|
NP_001311122.1:p.Arg24Trp
|
|
NM_024960.6:c.505A>T
|
NP_079236.3:p.Arg169Trp
|
|
NR_136715.2:n.949A>T
|
|
|
NM_001386393.1:c.1048A>T
MANE Select
|
NP_001373322.1:p.Arg350Trp
|
|
NM_153638.4:c.1378A>T
|
NP_705902.2:p.Arg460Trp
|
|
NM_153640.4:c.505A>T
|
NP_705904.1:p.Arg169Trp
|
|