ENST00000373344.11:c.7297C>A
MANE Select
|
ENSP00000362441.4:p.Leu2433Met
|
|
ENST00000675732.1:c.2395C>A
|
ENSP00000502598.1:p.Leu799Met
|
|
ENST00000373344.9:c.7297C>A
|
ENSP00000362441.4:p.Leu2433Met
|
|
ENST00000395603.7:c.7183C>A
|
ENSP00000378967.3:p.Leu2395Met
|
|
ENST00000480283.5:c.*6925C>A
|
ENSP00000480196.1:n.*6925C>A
|
|
ENST00000623706.3:n.5617C>A
|
|
|
ENST00000624766.1:n.528C>A
|
|
|
NM_000489.4:c.7297C>A
|
NP_000480.3:p.Leu2433Met
|
|
NM_138270.3:c.7183C>A
|
NP_612114.2:p.Leu2395Met
|
|
XM_005262153.3:c.7294C>A
|
XP_005262210.2:p.Leu2432Met
|
|
XM_005262154.3:c.7210C>A
|
XP_005262211.2:p.Leu2404Met
|
|
XM_005262155.3:c.7180C>A
|
XP_005262212.2:p.Leu2394Met
|
|
XM_005262156.3:c.7132C>A
|
XP_005262213.2:p.Leu2378Met
|
|
XM_005262157.3:c.7093C>A
|
XP_005262214.2:p.Leu2365Met
|
|
XM_006724666.2:c.7180C>A
|
XP_006724729.1:p.Leu2394Met
|
|
XM_006724667.2:c.7018C>A
|
XP_006724730.1:p.Leu2340Met
|
|
XR_938400.1:n.8889C>A
|
|
|
NM_000489.5:c.7297C>A
|
NP_000480.3:p.Leu2433Met
|
|
XM_005262153.5:c.7294C>A
|
XP_005262210.2:p.Leu2432Met
|
|
XM_005262154.5:c.7210C>A
|
XP_005262211.2:p.Leu2404Met
|
|
XM_005262155.4:c.7180C>A
|
XP_005262212.2:p.Leu2394Met
|
|
XM_005262156.4:c.7132C>A
|
XP_005262213.2:p.Leu2378Met
|
|
XM_005262157.5:c.7093C>A
|
XP_005262214.2:p.Leu2365Met
|
|
XM_006724666.4:c.7180C>A
|
XP_006724729.1:p.Leu2394Met
|
|
XM_006724667.3:c.7018C>A
|
XP_006724730.1:p.Leu2340Met
|
|
XM_017029601.2:c.7207C>A
|
XP_016885090.1:p.Leu2403Met
|
|
XM_017029602.1:c.7177C>A
|
XP_016885091.1:p.Leu2393Met
|
|
XM_017029603.1:c.7129C>A
|
XP_016885092.1:p.Leu2377Met
|
|
XM_017029604.2:c.7096C>A
|
XP_016885093.1:p.Leu2366Met
|
|
XM_017029605.1:c.7093C>A
|
XP_016885094.1:p.Leu2365Met
|
|
XM_017029606.2:c.7066C>A
|
XP_016885095.1:p.Leu2356Met
|
|
XM_017029607.2:c.7063C>A
|
XP_016885096.1:p.Leu2355Met
|
|
XM_017029608.2:c.7015C>A
|
XP_016885097.1:p.Leu2339Met
|
|
XM_017029609.1:c.6979C>A
|
XP_016885098.1:p.Leu2327Met
|
|
XM_017029610.1:c.6976C>A
|
XP_016885099.1:p.Leu2326Met
|
|
XM_017029611.1:c.6931C>A
|
XP_016885100.1:p.Leu2311Met
|
|
XR_001755700.2:n.7596C>A
|
|
|
NM_138270.4:c.7183C>A
|
NP_612114.2:p.Leu2395Met
|
|
NM_000489.6:c.7297C>A
MANE Select
|
NP_000480.3:p.Leu2433Met
|
|
NM_138270.5:c.7183C>A
|
NP_612114.2:p.Leu2395Met
|
|