ENST00000373344.11:c.7337T>G
MANE Select
|
ENSP00000362441.4:p.Met2446Arg
|
|
ENST00000675732.1:c.2435T>G
|
ENSP00000502598.1:p.Met812Arg
|
|
ENST00000373344.9:c.7337T>G
|
ENSP00000362441.4:p.Met2446Arg
|
|
ENST00000395603.7:c.7223T>G
|
ENSP00000378967.3:p.Met2408Arg
|
|
ENST00000480283.5:c.*6965T>G
|
ENSP00000480196.1:n.*6965T>G
|
|
ENST00000623706.3:n.5657T>G
|
|
|
ENST00000624766.1:n.568T>G
|
|
|
NM_000489.4:c.7337T>G
|
NP_000480.3:p.Met2446Arg
|
|
NM_138270.3:c.7223T>G
|
NP_612114.2:p.Met2408Arg
|
|
XM_005262153.3:c.7334T>G
|
XP_005262210.2:p.Met2445Arg
|
|
XM_005262154.3:c.7250T>G
|
XP_005262211.2:p.Met2417Arg
|
|
XM_005262155.3:c.7220T>G
|
XP_005262212.2:p.Met2407Arg
|
|
XM_005262156.3:c.7172T>G
|
XP_005262213.2:p.Met2391Arg
|
|
XM_005262157.3:c.7133T>G
|
XP_005262214.2:p.Met2378Arg
|
|
XM_006724666.2:c.7220T>G
|
XP_006724729.1:p.Met2407Arg
|
|
XM_006724667.2:c.7058T>G
|
XP_006724730.1:p.Met2353Arg
|
|
XR_938400.1:n.8929T>G
|
|
|
NM_000489.5:c.7337T>G
|
NP_000480.3:p.Met2446Arg
|
|
XM_005262153.5:c.7334T>G
|
XP_005262210.2:p.Met2445Arg
|
|
XM_005262154.5:c.7250T>G
|
XP_005262211.2:p.Met2417Arg
|
|
XM_005262155.4:c.7220T>G
|
XP_005262212.2:p.Met2407Arg
|
|
XM_005262156.4:c.7172T>G
|
XP_005262213.2:p.Met2391Arg
|
|
XM_005262157.5:c.7133T>G
|
XP_005262214.2:p.Met2378Arg
|
|
XM_006724666.4:c.7220T>G
|
XP_006724729.1:p.Met2407Arg
|
|
XM_006724667.3:c.7058T>G
|
XP_006724730.1:p.Met2353Arg
|
|
XM_017029601.2:c.7247T>G
|
XP_016885090.1:p.Met2416Arg
|
|
XM_017029602.1:c.7217T>G
|
XP_016885091.1:p.Met2406Arg
|
|
XM_017029603.1:c.7169T>G
|
XP_016885092.1:p.Met2390Arg
|
|
XM_017029604.2:c.7136T>G
|
XP_016885093.1:p.Met2379Arg
|
|
XM_017029605.1:c.7133T>G
|
XP_016885094.1:p.Met2378Arg
|
|
XM_017029606.2:c.7106T>G
|
XP_016885095.1:p.Met2369Arg
|
|
XM_017029607.2:c.7103T>G
|
XP_016885096.1:p.Met2368Arg
|
|
XM_017029608.2:c.7055T>G
|
XP_016885097.1:p.Met2352Arg
|
|
XM_017029609.1:c.7019T>G
|
XP_016885098.1:p.Met2340Arg
|
|
XM_017029610.1:c.7016T>G
|
XP_016885099.1:p.Met2339Arg
|
|
XM_017029611.1:c.6971T>G
|
XP_016885100.1:p.Met2324Arg
|
|
XR_001755700.2:n.7636T>G
|
|
|
NM_138270.4:c.7223T>G
|
NP_612114.2:p.Met2408Arg
|
|
NM_000489.6:c.7337T>G
MANE Select
|
NP_000480.3:p.Met2446Arg
|
|
NM_138270.5:c.7223T>G
|
NP_612114.2:p.Met2408Arg
|
|