ENST00000373344.11:c.7303C>G
MANE Select
|
ENSP00000362441.4:p.His2435Asp
|
|
ENST00000675732.1:c.2401C>G
|
ENSP00000502598.1:p.His801Asp
|
|
ENST00000373344.9:c.7303C>G
|
ENSP00000362441.4:p.His2435Asp
|
|
ENST00000395603.7:c.7189C>G
|
ENSP00000378967.3:p.His2397Asp
|
|
ENST00000480283.5:c.*6931C>G
|
ENSP00000480196.1:n.*6931C>G
|
|
ENST00000623706.3:n.5623C>G
|
|
|
ENST00000624766.1:n.534C>G
|
|
|
NM_000489.4:c.7303C>G
|
NP_000480.3:p.His2435Asp
|
|
NM_138270.3:c.7189C>G
|
NP_612114.2:p.His2397Asp
|
|
XM_005262153.3:c.7300C>G
|
XP_005262210.2:p.His2434Asp
|
|
XM_005262154.3:c.7216C>G
|
XP_005262211.2:p.His2406Asp
|
|
XM_005262155.3:c.7186C>G
|
XP_005262212.2:p.His2396Asp
|
|
XM_005262156.3:c.7138C>G
|
XP_005262213.2:p.His2380Asp
|
|
XM_005262157.3:c.7099C>G
|
XP_005262214.2:p.His2367Asp
|
|
XM_006724666.2:c.7186C>G
|
XP_006724729.1:p.His2396Asp
|
|
XM_006724667.2:c.7024C>G
|
XP_006724730.1:p.His2342Asp
|
|
XR_938400.1:n.8895C>G
|
|
|
NM_000489.5:c.7303C>G
|
NP_000480.3:p.His2435Asp
|
|
XM_005262153.5:c.7300C>G
|
XP_005262210.2:p.His2434Asp
|
|
XM_005262154.5:c.7216C>G
|
XP_005262211.2:p.His2406Asp
|
|
XM_005262155.4:c.7186C>G
|
XP_005262212.2:p.His2396Asp
|
|
XM_005262156.4:c.7138C>G
|
XP_005262213.2:p.His2380Asp
|
|
XM_005262157.5:c.7099C>G
|
XP_005262214.2:p.His2367Asp
|
|
XM_006724666.4:c.7186C>G
|
XP_006724729.1:p.His2396Asp
|
|
XM_006724667.3:c.7024C>G
|
XP_006724730.1:p.His2342Asp
|
|
XM_017029601.2:c.7213C>G
|
XP_016885090.1:p.His2405Asp
|
|
XM_017029602.1:c.7183C>G
|
XP_016885091.1:p.His2395Asp
|
|
XM_017029603.1:c.7135C>G
|
XP_016885092.1:p.His2379Asp
|
|
XM_017029604.2:c.7102C>G
|
XP_016885093.1:p.His2368Asp
|
|
XM_017029605.1:c.7099C>G
|
XP_016885094.1:p.His2367Asp
|
|
XM_017029606.2:c.7072C>G
|
XP_016885095.1:p.His2358Asp
|
|
XM_017029607.2:c.7069C>G
|
XP_016885096.1:p.His2357Asp
|
|
XM_017029608.2:c.7021C>G
|
XP_016885097.1:p.His2341Asp
|
|
XM_017029609.1:c.6985C>G
|
XP_016885098.1:p.His2329Asp
|
|
XM_017029610.1:c.6982C>G
|
XP_016885099.1:p.His2328Asp
|
|
XM_017029611.1:c.6937C>G
|
XP_016885100.1:p.His2313Asp
|
|
XR_001755700.2:n.7602C>G
|
|
|
NM_138270.4:c.7189C>G
|
NP_612114.2:p.His2397Asp
|
|
NM_000489.6:c.7303C>G
MANE Select
|
NP_000480.3:p.His2435Asp
|
|
NM_138270.5:c.7189C>G
|
NP_612114.2:p.His2397Asp
|
|