ENST00000373344.11:c.4456G>T
MANE Select
|
ENSP00000362441.4:p.Asp1486Tyr
|
|
ENST00000373344.9:c.4456G>T
|
ENSP00000362441.4:p.Asp1486Tyr
|
|
ENST00000395603.7:c.4342G>T
|
ENSP00000378967.3:p.Asp1448Tyr
|
|
ENST00000480283.5:c.*4084G>T
|
ENSP00000480196.1:n.*4084G>T
|
|
ENST00000623242.3:c.62G>T
|
|
|
NM_000489.4:c.4456G>T
|
NP_000480.3:p.Asp1486Tyr
|
|
NM_138270.3:c.4342G>T
|
NP_612114.2:p.Asp1448Tyr
|
|
XM_005262153.3:c.4453G>T
|
XP_005262210.2:p.Asp1485Tyr
|
|
XM_005262154.3:c.4369G>T
|
XP_005262211.2:p.Asp1457Tyr
|
|
XM_005262155.3:c.4339G>T
|
XP_005262212.2:p.Asp1447Tyr
|
|
XM_005262156.3:c.4291G>T
|
XP_005262213.2:p.Asp1431Tyr
|
|
XM_005262157.3:c.4252G>T
|
XP_005262214.2:p.Asp1418Tyr
|
|
XM_006724666.2:c.4339G>T
|
XP_006724729.1:p.Asp1447Tyr
|
|
XM_006724667.2:c.4177G>T
|
XP_006724730.1:p.Asp1393Tyr
|
|
XM_006724668.2:c.4456G>T
|
XP_006724731.1:p.Asp1486Tyr
|
|
XR_938400.1:n.4724G>T
|
|
|
NM_000489.5:c.4456G>T
|
NP_000480.3:p.Asp1486Tyr
|
|
XM_005262153.5:c.4453G>T
|
XP_005262210.2:p.Asp1485Tyr
|
|
XM_005262154.5:c.4369G>T
|
XP_005262211.2:p.Asp1457Tyr
|
|
XM_005262155.4:c.4339G>T
|
XP_005262212.2:p.Asp1447Tyr
|
|
XM_005262156.4:c.4291G>T
|
XP_005262213.2:p.Asp1431Tyr
|
|
XM_005262157.5:c.4252G>T
|
XP_005262214.2:p.Asp1418Tyr
|
|
XM_006724666.4:c.4339G>T
|
XP_006724729.1:p.Asp1447Tyr
|
|
XM_006724667.3:c.4177G>T
|
XP_006724730.1:p.Asp1393Tyr
|
|
XM_006724668.3:c.4456G>T
|
XP_006724731.1:p.Asp1486Tyr
|
|
XM_017029601.2:c.4366G>T
|
XP_016885090.1:p.Asp1456Tyr
|
|
XM_017029602.1:c.4336G>T
|
XP_016885091.1:p.Asp1446Tyr
|
|
XM_017029603.1:c.4288G>T
|
XP_016885092.1:p.Asp1430Tyr
|
|
XM_017029604.2:c.4255G>T
|
XP_016885093.1:p.Asp1419Tyr
|
|
XM_017029605.1:c.4252G>T
|
XP_016885094.1:p.Asp1418Tyr
|
|
XM_017029606.2:c.4225G>T
|
XP_016885095.1:p.Asp1409Tyr
|
|
XM_017029607.2:c.4222G>T
|
XP_016885096.1:p.Asp1408Tyr
|
|
XM_017029608.2:c.4174G>T
|
XP_016885097.1:p.Asp1392Tyr
|
|
XM_017029609.1:c.4138G>T
|
XP_016885098.1:p.Asp1380Tyr
|
|
XM_017029610.1:c.4135G>T
|
XP_016885099.1:p.Asp1379Tyr
|
|
XM_017029611.1:c.4090G>T
|
XP_016885100.1:p.Asp1364Tyr
|
|
XR_001755700.2:n.4681G>T
|
|
|
NM_138270.4:c.4342G>T
|
NP_612114.2:p.Asp1448Tyr
|
|
NM_000489.6:c.4456G>T
MANE Select
|
NP_000480.3:p.Asp1486Tyr
|
|
NM_138270.5:c.4342G>T
|
NP_612114.2:p.Asp1448Tyr
|
|