ENST00000373344.11:c.4393G>A
MANE Select
|
ENSP00000362441.4:p.Asp1465Asn
|
|
ENST00000373344.9:c.4393G>A
|
ENSP00000362441.4:p.Asp1465Asn
|
|
ENST00000395603.7:c.4279G>A
|
ENSP00000378967.3:p.Asp1427Asn
|
|
ENST00000480283.5:c.*4021G>A
|
ENSP00000480196.1:n.*4021G>A
|
|
NM_000489.4:c.4393G>A
|
NP_000480.3:p.Asp1465Asn
|
|
NM_138270.3:c.4279G>A
|
NP_612114.2:p.Asp1427Asn
|
|
XM_005262153.3:c.4390G>A
|
XP_005262210.2:p.Asp1464Asn
|
|
XM_005262154.3:c.4306G>A
|
XP_005262211.2:p.Asp1436Asn
|
|
XM_005262155.3:c.4276G>A
|
XP_005262212.2:p.Asp1426Asn
|
|
XM_005262156.3:c.4228G>A
|
XP_005262213.2:p.Asp1410Asn
|
|
XM_005262157.3:c.4189G>A
|
XP_005262214.2:p.Asp1397Asn
|
|
XM_006724666.2:c.4276G>A
|
XP_006724729.1:p.Asp1426Asn
|
|
XM_006724667.2:c.4114G>A
|
XP_006724730.1:p.Asp1372Asn
|
|
XM_006724668.2:c.4393G>A
|
XP_006724731.1:p.Asp1465Asn
|
|
XR_938400.1:n.4661G>A
|
|
|
NM_000489.5:c.4393G>A
|
NP_000480.3:p.Asp1465Asn
|
|
XM_005262153.5:c.4390G>A
|
XP_005262210.2:p.Asp1464Asn
|
|
XM_005262154.5:c.4306G>A
|
XP_005262211.2:p.Asp1436Asn
|
|
XM_005262155.4:c.4276G>A
|
XP_005262212.2:p.Asp1426Asn
|
|
XM_005262156.4:c.4228G>A
|
XP_005262213.2:p.Asp1410Asn
|
|
XM_005262157.5:c.4189G>A
|
XP_005262214.2:p.Asp1397Asn
|
|
XM_006724666.4:c.4276G>A
|
XP_006724729.1:p.Asp1426Asn
|
|
XM_006724667.3:c.4114G>A
|
XP_006724730.1:p.Asp1372Asn
|
|
XM_006724668.3:c.4393G>A
|
XP_006724731.1:p.Asp1465Asn
|
|
XM_017029601.2:c.4303G>A
|
XP_016885090.1:p.Asp1435Asn
|
|
XM_017029602.1:c.4273G>A
|
XP_016885091.1:p.Asp1425Asn
|
|
XM_017029603.1:c.4225G>A
|
XP_016885092.1:p.Asp1409Asn
|
|
XM_017029604.2:c.4192G>A
|
XP_016885093.1:p.Asp1398Asn
|
|
XM_017029605.1:c.4189G>A
|
XP_016885094.1:p.Asp1397Asn
|
|
XM_017029606.2:c.4162G>A
|
XP_016885095.1:p.Asp1388Asn
|
|
XM_017029607.2:c.4159G>A
|
XP_016885096.1:p.Asp1387Asn
|
|
XM_017029608.2:c.4111G>A
|
XP_016885097.1:p.Asp1371Asn
|
|
XM_017029609.1:c.4075G>A
|
XP_016885098.1:p.Asp1359Asn
|
|
XM_017029610.1:c.4072G>A
|
XP_016885099.1:p.Asp1358Asn
|
|
XM_017029611.1:c.4027G>A
|
XP_016885100.1:p.Asp1343Asn
|
|
XR_001755700.2:n.4618G>A
|
|
|
NM_138270.4:c.4279G>A
|
NP_612114.2:p.Asp1427Asn
|
|
NM_000489.6:c.4393G>A
MANE Select
|
NP_000480.3:p.Asp1465Asn
|
|
NM_138270.5:c.4279G>A
|
NP_612114.2:p.Asp1427Asn
|
|