ENST00000373344.11:c.7309A>G
MANE Select
|
ENSP00000362441.4:p.Met2437Val
|
|
ENST00000675732.1:c.2407A>G
|
ENSP00000502598.1:p.Met803Val
|
|
ENST00000373344.9:c.7309A>G
|
ENSP00000362441.4:p.Met2437Val
|
|
ENST00000395603.7:c.7195A>G
|
ENSP00000378967.3:p.Met2399Val
|
|
ENST00000480283.5:c.*6937A>G
|
ENSP00000480196.1:n.*6937A>G
|
|
ENST00000623706.3:n.5629A>G
|
|
|
ENST00000624766.1:n.540A>G
|
|
|
NM_000489.4:c.7309A>G
|
NP_000480.3:p.Met2437Val
|
|
NM_138270.3:c.7195A>G
|
NP_612114.2:p.Met2399Val
|
|
XM_005262153.3:c.7306A>G
|
XP_005262210.2:p.Met2436Val
|
|
XM_005262154.3:c.7222A>G
|
XP_005262211.2:p.Met2408Val
|
|
XM_005262155.3:c.7192A>G
|
XP_005262212.2:p.Met2398Val
|
|
XM_005262156.3:c.7144A>G
|
XP_005262213.2:p.Met2382Val
|
|
XM_005262157.3:c.7105A>G
|
XP_005262214.2:p.Met2369Val
|
|
XM_006724666.2:c.7192A>G
|
XP_006724729.1:p.Met2398Val
|
|
XM_006724667.2:c.7030A>G
|
XP_006724730.1:p.Met2344Val
|
|
XR_938400.1:n.8901A>G
|
|
|
NM_000489.5:c.7309A>G
|
NP_000480.3:p.Met2437Val
|
|
XM_005262153.5:c.7306A>G
|
XP_005262210.2:p.Met2436Val
|
|
XM_005262154.5:c.7222A>G
|
XP_005262211.2:p.Met2408Val
|
|
XM_005262155.4:c.7192A>G
|
XP_005262212.2:p.Met2398Val
|
|
XM_005262156.4:c.7144A>G
|
XP_005262213.2:p.Met2382Val
|
|
XM_005262157.5:c.7105A>G
|
XP_005262214.2:p.Met2369Val
|
|
XM_006724666.4:c.7192A>G
|
XP_006724729.1:p.Met2398Val
|
|
XM_006724667.3:c.7030A>G
|
XP_006724730.1:p.Met2344Val
|
|
XM_017029601.2:c.7219A>G
|
XP_016885090.1:p.Met2407Val
|
|
XM_017029602.1:c.7189A>G
|
XP_016885091.1:p.Met2397Val
|
|
XM_017029603.1:c.7141A>G
|
XP_016885092.1:p.Met2381Val
|
|
XM_017029604.2:c.7108A>G
|
XP_016885093.1:p.Met2370Val
|
|
XM_017029605.1:c.7105A>G
|
XP_016885094.1:p.Met2369Val
|
|
XM_017029606.2:c.7078A>G
|
XP_016885095.1:p.Met2360Val
|
|
XM_017029607.2:c.7075A>G
|
XP_016885096.1:p.Met2359Val
|
|
XM_017029608.2:c.7027A>G
|
XP_016885097.1:p.Met2343Val
|
|
XM_017029609.1:c.6991A>G
|
XP_016885098.1:p.Met2331Val
|
|
XM_017029610.1:c.6988A>G
|
XP_016885099.1:p.Met2330Val
|
|
XM_017029611.1:c.6943A>G
|
XP_016885100.1:p.Met2315Val
|
|
XR_001755700.2:n.7608A>G
|
|
|
NM_138270.4:c.7195A>G
|
NP_612114.2:p.Met2399Val
|
|
NM_000489.6:c.7309A>G
MANE Select
|
NP_000480.3:p.Met2437Val
|
|
NM_138270.5:c.7195A>G
|
NP_612114.2:p.Met2399Val
|
|