ENST00000285021.12:c.2193C>T
MANE Select
|
ENSP00000285021.8:p.Gly731=
|
|
ENST00000285021.11:c.2193C>T
|
ENSP00000285021.7:p.Gly731=
|
|
ENST00000427795.2:n.58C>T
|
|
|
ENST00000476581.6:c.*1646C>T
|
ENSP00000424548.1:n.*1646C>T
|
|
NM_004628.4:c.2193C>T , LRG_472t1:c.2193C>T
|
NP_004619.3:p.Gly731=
|
|
NR_027299.1:n.2173C>T
|
|
|
XM_011534092.1:c.2193C>T
|
XP_011532394.1:p.Gly731=
|
|
NM_001354726.1:c.1614C>T
|
NP_001341655.1:p.Gly538=
|
|
NM_001354727.1:c.2187C>T
|
NP_001341656.1:p.Gly729=
|
|
NM_001354729.1:c.2175C>T
|
NP_001341658.1:p.Gly725=
|
|
NM_001354730.1:c.1947C>T
|
NP_001341659.1:p.Gly649=
|
|
NR_148950.1:n.2136C>T
|
|
|
NR_148951.1:n.2012C>T
|
|
|
XR_001740256.2:n.2226C>T
|
|
|
XR_002959580.1:n.2226C>T
|
|
|
XR_002959581.1:n.3843C>T
|
|
|
NM_001354727.2:c.2187C>T
|
NP_001341656.1:p.Gly729=
|
|
NM_004628.5:c.2193C>T
MANE Select
|
NP_004619.3:p.Gly731=
|
|
NR_148950.2:n.2065C>T
|
|
|
NR_148951.2:n.1941C>T
|
|
|
NM_001354726.2:c.1614C>T
|
NP_001341655.1:p.Gly538=
|
|
NM_001354729.2:c.2175C>T
|
NP_001341658.1:p.Gly725=
|
|
NM_001354730.2:c.1947C>T
|
NP_001341659.1:p.Gly649=
|
|