ENST00000373344.11:c.7328A>G
MANE Select
|
ENSP00000362441.4:p.Asn2443Ser
|
|
ENST00000675732.1:c.2426A>G
|
ENSP00000502598.1:p.Asn809Ser
|
|
ENST00000373344.9:c.7328A>G
|
ENSP00000362441.4:p.Asn2443Ser
|
|
ENST00000395603.7:c.7214A>G
|
ENSP00000378967.3:p.Asn2405Ser
|
|
ENST00000480283.5:c.*6956A>G
|
ENSP00000480196.1:n.*6956A>G
|
|
ENST00000623706.3:n.5648A>G
|
|
|
ENST00000624766.1:n.559A>G
|
|
|
NM_000489.4:c.7328A>G
|
NP_000480.3:p.Asn2443Ser
|
|
NM_138270.3:c.7214A>G
|
NP_612114.2:p.Asn2405Ser
|
|
XM_005262153.3:c.7325A>G
|
XP_005262210.2:p.Asn2442Ser
|
|
XM_005262154.3:c.7241A>G
|
XP_005262211.2:p.Asn2414Ser
|
|
XM_005262155.3:c.7211A>G
|
XP_005262212.2:p.Asn2404Ser
|
|
XM_005262156.3:c.7163A>G
|
XP_005262213.2:p.Asn2388Ser
|
|
XM_005262157.3:c.7124A>G
|
XP_005262214.2:p.Asn2375Ser
|
|
XM_006724666.2:c.7211A>G
|
XP_006724729.1:p.Asn2404Ser
|
|
XM_006724667.2:c.7049A>G
|
XP_006724730.1:p.Asn2350Ser
|
|
XR_938400.1:n.8920A>G
|
|
|
NM_000489.5:c.7328A>G
|
NP_000480.3:p.Asn2443Ser
|
|
XM_005262153.5:c.7325A>G
|
XP_005262210.2:p.Asn2442Ser
|
|
XM_005262154.5:c.7241A>G
|
XP_005262211.2:p.Asn2414Ser
|
|
XM_005262155.4:c.7211A>G
|
XP_005262212.2:p.Asn2404Ser
|
|
XM_005262156.4:c.7163A>G
|
XP_005262213.2:p.Asn2388Ser
|
|
XM_005262157.5:c.7124A>G
|
XP_005262214.2:p.Asn2375Ser
|
|
XM_006724666.4:c.7211A>G
|
XP_006724729.1:p.Asn2404Ser
|
|
XM_006724667.3:c.7049A>G
|
XP_006724730.1:p.Asn2350Ser
|
|
XM_017029601.2:c.7238A>G
|
XP_016885090.1:p.Asn2413Ser
|
|
XM_017029602.1:c.7208A>G
|
XP_016885091.1:p.Asn2403Ser
|
|
XM_017029603.1:c.7160A>G
|
XP_016885092.1:p.Asn2387Ser
|
|
XM_017029604.2:c.7127A>G
|
XP_016885093.1:p.Asn2376Ser
|
|
XM_017029605.1:c.7124A>G
|
XP_016885094.1:p.Asn2375Ser
|
|
XM_017029606.2:c.7097A>G
|
XP_016885095.1:p.Asn2366Ser
|
|
XM_017029607.2:c.7094A>G
|
XP_016885096.1:p.Asn2365Ser
|
|
XM_017029608.2:c.7046A>G
|
XP_016885097.1:p.Asn2349Ser
|
|
XM_017029609.1:c.7010A>G
|
XP_016885098.1:p.Asn2337Ser
|
|
XM_017029610.1:c.7007A>G
|
XP_016885099.1:p.Asn2336Ser
|
|
XM_017029611.1:c.6962A>G
|
XP_016885100.1:p.Asn2321Ser
|
|
XR_001755700.2:n.7627A>G
|
|
|
NM_138270.4:c.7214A>G
|
NP_612114.2:p.Asn2405Ser
|
|
NM_000489.6:c.7328A>G
MANE Select
|
NP_000480.3:p.Asn2443Ser
|
|
NM_138270.5:c.7214A>G
|
NP_612114.2:p.Asn2405Ser
|
|