ENST00000373344.11:c.7283A>G
MANE Select
|
ENSP00000362441.4:p.Tyr2428Cys
|
|
ENST00000675732.1:c.2381A>G
|
ENSP00000502598.1:p.Tyr794Cys
|
|
ENST00000373344.9:c.7283A>G
|
ENSP00000362441.4:p.Tyr2428Cys
|
|
ENST00000395603.7:c.7169A>G
|
ENSP00000378967.3:p.Tyr2390Cys
|
|
ENST00000480283.5:c.*6911A>G
|
ENSP00000480196.1:n.*6911A>G
|
|
ENST00000623706.3:n.5603A>G
|
|
|
ENST00000624766.1:n.514A>G
|
|
|
NM_000489.4:c.7283A>G
|
NP_000480.3:p.Tyr2428Cys
|
|
NM_138270.3:c.7169A>G
|
NP_612114.2:p.Tyr2390Cys
|
|
XM_005262153.3:c.7280A>G
|
XP_005262210.2:p.Tyr2427Cys
|
|
XM_005262154.3:c.7196A>G
|
XP_005262211.2:p.Tyr2399Cys
|
|
XM_005262155.3:c.7166A>G
|
XP_005262212.2:p.Tyr2389Cys
|
|
XM_005262156.3:c.7118A>G
|
XP_005262213.2:p.Tyr2373Cys
|
|
XM_005262157.3:c.7079A>G
|
XP_005262214.2:p.Tyr2360Cys
|
|
XM_006724666.2:c.7166A>G
|
XP_006724729.1:p.Tyr2389Cys
|
|
XM_006724667.2:c.7004A>G
|
XP_006724730.1:p.Tyr2335Cys
|
|
XR_938400.1:n.8875A>G
|
|
|
NM_000489.5:c.7283A>G
|
NP_000480.3:p.Tyr2428Cys
|
|
XM_005262153.5:c.7280A>G
|
XP_005262210.2:p.Tyr2427Cys
|
|
XM_005262154.5:c.7196A>G
|
XP_005262211.2:p.Tyr2399Cys
|
|
XM_005262155.4:c.7166A>G
|
XP_005262212.2:p.Tyr2389Cys
|
|
XM_005262156.4:c.7118A>G
|
XP_005262213.2:p.Tyr2373Cys
|
|
XM_005262157.5:c.7079A>G
|
XP_005262214.2:p.Tyr2360Cys
|
|
XM_006724666.4:c.7166A>G
|
XP_006724729.1:p.Tyr2389Cys
|
|
XM_006724667.3:c.7004A>G
|
XP_006724730.1:p.Tyr2335Cys
|
|
XM_017029601.2:c.7193A>G
|
XP_016885090.1:p.Tyr2398Cys
|
|
XM_017029602.1:c.7163A>G
|
XP_016885091.1:p.Tyr2388Cys
|
|
XM_017029603.1:c.7115A>G
|
XP_016885092.1:p.Tyr2372Cys
|
|
XM_017029604.2:c.7082A>G
|
XP_016885093.1:p.Tyr2361Cys
|
|
XM_017029605.1:c.7079A>G
|
XP_016885094.1:p.Tyr2360Cys
|
|
XM_017029606.2:c.7052A>G
|
XP_016885095.1:p.Tyr2351Cys
|
|
XM_017029607.2:c.7049A>G
|
XP_016885096.1:p.Tyr2350Cys
|
|
XM_017029608.2:c.7001A>G
|
XP_016885097.1:p.Tyr2334Cys
|
|
XM_017029609.1:c.6965A>G
|
XP_016885098.1:p.Tyr2322Cys
|
|
XM_017029610.1:c.6962A>G
|
XP_016885099.1:p.Tyr2321Cys
|
|
XM_017029611.1:c.6917A>G
|
XP_016885100.1:p.Tyr2306Cys
|
|
XR_001755700.2:n.7582A>G
|
|
|
NM_138270.4:c.7169A>G
|
NP_612114.2:p.Tyr2390Cys
|
|
NM_000489.6:c.7283A>G
MANE Select
|
NP_000480.3:p.Tyr2428Cys
|
|
NM_138270.5:c.7169A>G
|
NP_612114.2:p.Tyr2390Cys
|
|