ENST00000356231.4:c.3329C>G
MANE Select
|
ENSP00000348564.3:p.Ala1110Gly
|
|
ENST00000643434.1:c.*2396C>G
|
ENSP00000494699.1:n.*2396C>G
|
|
ENST00000356231.3:c.3329C>G
|
ENSP00000348564.3:p.Ala1110Gly
|
|
ENST00000562465.5:c.1275C>G
|
ENSP00000454246.1:n.1275C>G
|
|
ENST00000563604.1:n.28C>G
|
|
|
NM_138477.2:c.3329C>G
|
NP_612486.2:p.Ala1110Gly
|
|
XM_005254176.3:c.3332C>G
|
XP_005254233.1:p.Ala1111Gly
|
|
XM_011521270.1:c.3356C>G
|
XP_011519572.1:p.Ala1119Gly
|
|
XM_011521271.1:c.3353C>G
|
XP_011519573.1:p.Ala1118Gly
|
|
XM_011521272.1:c.*37C>G
|
XP_011519574.1:n.*37C>G
|
|
XM_011521274.1:c.2321C>G
|
XP_011519576.1:p.Ala774Gly
|
|
XM_011521275.1:c.2573C>G
|
XP_011519577.1:p.Ala858Gly
|
|
NM_138477.4:c.3329C>G
MANE Select
|
NP_612486.2:p.Ala1110Gly
|
|
XM_005254176.5:c.3332C>G
|
XP_005254233.1:p.Ala1111Gly
|
|
XM_011521270.2:c.3356C>G
|
XP_011519572.1:p.Ala1119Gly
|
|
XM_011521271.2:c.3353C>G
|
XP_011519573.1:p.Ala1118Gly
|
|
XM_011521274.2:c.2321C>G
|
XP_011519576.1:p.Ala774Gly
|
|
XR_001751104.1:n.3322C>G
|
|
|
XR_001751105.1:n.3339C>G
|
|
|