ENST00000373344.11:c.7340A>G
MANE Select
|
ENSP00000362441.4:p.Asn2447Ser
|
|
ENST00000675732.1:c.2438A>G
|
ENSP00000502598.1:p.Asn813Ser
|
|
ENST00000373344.9:c.7340A>G
|
ENSP00000362441.4:p.Asn2447Ser
|
|
ENST00000395603.7:c.7226A>G
|
ENSP00000378967.3:p.Asn2409Ser
|
|
ENST00000480283.5:c.*6968A>G
|
ENSP00000480196.1:n.*6968A>G
|
|
ENST00000623706.3:n.5660A>G
|
|
|
ENST00000624766.1:n.571A>G
|
|
|
NM_000489.4:c.7340A>G
|
NP_000480.3:p.Asn2447Ser
|
|
NM_138270.3:c.7226A>G
|
NP_612114.2:p.Asn2409Ser
|
|
XM_005262153.3:c.7337A>G
|
XP_005262210.2:p.Asn2446Ser
|
|
XM_005262154.3:c.7253A>G
|
XP_005262211.2:p.Asn2418Ser
|
|
XM_005262155.3:c.7223A>G
|
XP_005262212.2:p.Asn2408Ser
|
|
XM_005262156.3:c.7175A>G
|
XP_005262213.2:p.Asn2392Ser
|
|
XM_005262157.3:c.7136A>G
|
XP_005262214.2:p.Asn2379Ser
|
|
XM_006724666.2:c.7223A>G
|
XP_006724729.1:p.Asn2408Ser
|
|
XM_006724667.2:c.7061A>G
|
XP_006724730.1:p.Asn2354Ser
|
|
XR_938400.1:n.8932A>G
|
|
|
NM_000489.5:c.7340A>G
|
NP_000480.3:p.Asn2447Ser
|
|
XM_005262153.5:c.7337A>G
|
XP_005262210.2:p.Asn2446Ser
|
|
XM_005262154.5:c.7253A>G
|
XP_005262211.2:p.Asn2418Ser
|
|
XM_005262155.4:c.7223A>G
|
XP_005262212.2:p.Asn2408Ser
|
|
XM_005262156.4:c.7175A>G
|
XP_005262213.2:p.Asn2392Ser
|
|
XM_005262157.5:c.7136A>G
|
XP_005262214.2:p.Asn2379Ser
|
|
XM_006724666.4:c.7223A>G
|
XP_006724729.1:p.Asn2408Ser
|
|
XM_006724667.3:c.7061A>G
|
XP_006724730.1:p.Asn2354Ser
|
|
XM_017029601.2:c.7250A>G
|
XP_016885090.1:p.Asn2417Ser
|
|
XM_017029602.1:c.7220A>G
|
XP_016885091.1:p.Asn2407Ser
|
|
XM_017029603.1:c.7172A>G
|
XP_016885092.1:p.Asn2391Ser
|
|
XM_017029604.2:c.7139A>G
|
XP_016885093.1:p.Asn2380Ser
|
|
XM_017029605.1:c.7136A>G
|
XP_016885094.1:p.Asn2379Ser
|
|
XM_017029606.2:c.7109A>G
|
XP_016885095.1:p.Asn2370Ser
|
|
XM_017029607.2:c.7106A>G
|
XP_016885096.1:p.Asn2369Ser
|
|
XM_017029608.2:c.7058A>G
|
XP_016885097.1:p.Asn2353Ser
|
|
XM_017029609.1:c.7022A>G
|
XP_016885098.1:p.Asn2341Ser
|
|
XM_017029610.1:c.7019A>G
|
XP_016885099.1:p.Asn2340Ser
|
|
XM_017029611.1:c.6974A>G
|
XP_016885100.1:p.Asn2325Ser
|
|
XR_001755700.2:n.7639A>G
|
|
|
NM_138270.4:c.7226A>G
|
NP_612114.2:p.Asn2409Ser
|
|
NM_000489.6:c.7340A>G
MANE Select
|
NP_000480.3:p.Asn2447Ser
|
|
NM_138270.5:c.7226A>G
|
NP_612114.2:p.Asn2409Ser
|
|