ENST00000373344.11:c.7385C>G
MANE Select
|
ENSP00000362441.4:p.Pro2462Arg
|
|
ENST00000675732.1:c.2483C>G
|
ENSP00000502598.1:p.Pro828Arg
|
|
ENST00000373344.9:c.7385C>G
|
ENSP00000362441.4:p.Pro2462Arg
|
|
ENST00000395603.7:c.7271C>G
|
ENSP00000378967.3:p.Pro2424Arg
|
|
ENST00000480283.5:c.*7013C>G
|
ENSP00000480196.1:n.*7013C>G
|
|
ENST00000623706.3:n.5705C>G
|
|
|
NM_000489.4:c.7385C>G
|
NP_000480.3:p.Pro2462Arg
|
|
NM_138270.3:c.7271C>G
|
NP_612114.2:p.Pro2424Arg
|
|
XM_005262153.3:c.7382C>G
|
XP_005262210.2:p.Pro2461Arg
|
|
XM_005262154.3:c.7298C>G
|
XP_005262211.2:p.Pro2433Arg
|
|
XM_005262155.3:c.7268C>G
|
XP_005262212.2:p.Pro2423Arg
|
|
XM_005262156.3:c.7220C>G
|
XP_005262213.2:p.Pro2407Arg
|
|
XM_005262157.3:c.7181C>G
|
XP_005262214.2:p.Pro2394Arg
|
|
XM_006724666.2:c.7268C>G
|
XP_006724729.1:p.Pro2423Arg
|
|
XM_006724667.2:c.7106C>G
|
XP_006724730.1:p.Pro2369Arg
|
|
XR_938400.1:n.8977C>G
|
|
|
NM_000489.5:c.7385C>G
|
NP_000480.3:p.Pro2462Arg
|
|
XM_005262153.5:c.7382C>G
|
XP_005262210.2:p.Pro2461Arg
|
|
XM_005262154.5:c.7298C>G
|
XP_005262211.2:p.Pro2433Arg
|
|
XM_005262155.4:c.7268C>G
|
XP_005262212.2:p.Pro2423Arg
|
|
XM_005262156.4:c.7220C>G
|
XP_005262213.2:p.Pro2407Arg
|
|
XM_005262157.5:c.7181C>G
|
XP_005262214.2:p.Pro2394Arg
|
|
XM_006724666.4:c.7268C>G
|
XP_006724729.1:p.Pro2423Arg
|
|
XM_006724667.3:c.7106C>G
|
XP_006724730.1:p.Pro2369Arg
|
|
XM_017029601.2:c.7295C>G
|
XP_016885090.1:p.Pro2432Arg
|
|
XM_017029602.1:c.7265C>G
|
XP_016885091.1:p.Pro2422Arg
|
|
XM_017029603.1:c.7217C>G
|
XP_016885092.1:p.Pro2406Arg
|
|
XM_017029604.2:c.7184C>G
|
XP_016885093.1:p.Pro2395Arg
|
|
XM_017029605.1:c.7181C>G
|
XP_016885094.1:p.Pro2394Arg
|
|
XM_017029606.2:c.7154C>G
|
XP_016885095.1:p.Pro2385Arg
|
|
XM_017029607.2:c.7151C>G
|
XP_016885096.1:p.Pro2384Arg
|
|
XM_017029608.2:c.7103C>G
|
XP_016885097.1:p.Pro2368Arg
|
|
XM_017029609.1:c.7067C>G
|
XP_016885098.1:p.Pro2356Arg
|
|
XM_017029610.1:c.7064C>G
|
XP_016885099.1:p.Pro2355Arg
|
|
XM_017029611.1:c.7019C>G
|
XP_016885100.1:p.Pro2340Arg
|
|
XR_001755700.2:n.7684C>G
|
|
|
NM_138270.4:c.7271C>G
|
NP_612114.2:p.Pro2424Arg
|
|
NM_000489.6:c.7385C>G
MANE Select
|
NP_000480.3:p.Pro2462Arg
|
|
NM_138270.5:c.7271C>G
|
NP_612114.2:p.Pro2424Arg
|
|