ENST00000373344.11:c.7421G>T
MANE Select
|
ENSP00000362441.4:p.Arg2474Leu
|
|
ENST00000675732.1:c.2519G>T
|
ENSP00000502598.1:p.Arg840Leu
|
|
ENST00000373344.9:c.7421G>T
|
ENSP00000362441.4:p.Arg2474Leu
|
|
ENST00000395603.7:c.7307G>T
|
ENSP00000378967.3:p.Arg2436Leu
|
|
ENST00000480283.5:c.*7049G>T
|
ENSP00000480196.1:n.*7049G>T
|
|
ENST00000623706.3:n.5741G>T
|
|
|
NM_000489.4:c.7421G>T
|
NP_000480.3:p.Arg2474Leu
|
|
NM_138270.3:c.7307G>T
|
NP_612114.2:p.Arg2436Leu
|
|
XM_005262153.3:c.7418G>T
|
XP_005262210.2:p.Arg2473Leu
|
|
XM_005262154.3:c.7334G>T
|
XP_005262211.2:p.Arg2445Leu
|
|
XM_005262155.3:c.7304G>T
|
XP_005262212.2:p.Arg2435Leu
|
|
XM_005262156.3:c.7256G>T
|
XP_005262213.2:p.Arg2419Leu
|
|
XM_005262157.3:c.7217G>T
|
XP_005262214.2:p.Arg2406Leu
|
|
XM_006724666.2:c.7304G>T
|
XP_006724729.1:p.Arg2435Leu
|
|
XM_006724667.2:c.7142G>T
|
XP_006724730.1:p.Arg2381Leu
|
|
XR_938400.1:n.9013G>T
|
|
|
NM_000489.5:c.7421G>T
|
NP_000480.3:p.Arg2474Leu
|
|
XM_005262153.5:c.7418G>T
|
XP_005262210.2:p.Arg2473Leu
|
|
XM_005262154.5:c.7334G>T
|
XP_005262211.2:p.Arg2445Leu
|
|
XM_005262155.4:c.7304G>T
|
XP_005262212.2:p.Arg2435Leu
|
|
XM_005262156.4:c.7256G>T
|
XP_005262213.2:p.Arg2419Leu
|
|
XM_005262157.5:c.7217G>T
|
XP_005262214.2:p.Arg2406Leu
|
|
XM_006724666.4:c.7304G>T
|
XP_006724729.1:p.Arg2435Leu
|
|
XM_006724667.3:c.7142G>T
|
XP_006724730.1:p.Arg2381Leu
|
|
XM_017029601.2:c.7331G>T
|
XP_016885090.1:p.Arg2444Leu
|
|
XM_017029602.1:c.7301G>T
|
XP_016885091.1:p.Arg2434Leu
|
|
XM_017029603.1:c.7253G>T
|
XP_016885092.1:p.Arg2418Leu
|
|
XM_017029604.2:c.7220G>T
|
XP_016885093.1:p.Arg2407Leu
|
|
XM_017029605.1:c.7217G>T
|
XP_016885094.1:p.Arg2406Leu
|
|
XM_017029606.2:c.7190G>T
|
XP_016885095.1:p.Arg2397Leu
|
|
XM_017029607.2:c.7187G>T
|
XP_016885096.1:p.Arg2396Leu
|
|
XM_017029608.2:c.7139G>T
|
XP_016885097.1:p.Arg2380Leu
|
|
XM_017029609.1:c.7103G>T
|
XP_016885098.1:p.Arg2368Leu
|
|
XM_017029610.1:c.7100G>T
|
XP_016885099.1:p.Arg2367Leu
|
|
XM_017029611.1:c.7055G>T
|
XP_016885100.1:p.Arg2352Leu
|
|
XR_001755700.2:n.7720G>T
|
|
|
NM_138270.4:c.7307G>T
|
NP_612114.2:p.Arg2436Leu
|
|
NM_000489.6:c.7421G>T
MANE Select
|
NP_000480.3:p.Arg2474Leu
|
|
NM_138270.5:c.7307G>T
|
NP_612114.2:p.Arg2436Leu
|
|