ENST00000285021.12:c.2232A>G
MANE Select
|
ENSP00000285021.8:p.Pro744=
|
|
ENST00000285021.11:c.2232A>G
|
ENSP00000285021.7:p.Pro744=
|
|
ENST00000427795.2:n.97A>G
|
|
|
ENST00000476581.6:c.*1685A>G
|
ENSP00000424548.1:n.*1685A>G
|
|
NM_004628.4:c.2232A>G , LRG_472t1:c.2232A>G
|
NP_004619.3:p.Pro744=
|
|
NR_027299.1:n.2212A>G
|
|
|
XM_011534092.1:c.2232A>G
|
XP_011532394.1:p.Pro744=
|
|
NM_001354726.1:c.1653A>G
|
NP_001341655.1:p.Pro551=
|
|
NM_001354727.1:c.2226A>G
|
NP_001341656.1:p.Pro742=
|
|
NM_001354729.1:c.2214A>G
|
NP_001341658.1:p.Pro738=
|
|
NM_001354730.1:c.1986A>G
|
NP_001341659.1:p.Pro662=
|
|
NR_148950.1:n.2175A>G
|
|
|
NR_148951.1:n.2051A>G
|
|
|
XR_001740256.2:n.2265A>G
|
|
|
XR_002959580.1:n.2265A>G
|
|
|
XR_002959581.1:n.3882A>G
|
|
|
NM_001354727.2:c.2226A>G
|
NP_001341656.1:p.Pro742=
|
|
NM_004628.5:c.2232A>G
MANE Select
|
NP_004619.3:p.Pro744=
|
|
NR_148950.2:n.2104A>G
|
|
|
NR_148951.2:n.1980A>G
|
|
|
NM_001354726.2:c.1653A>G
|
NP_001341655.1:p.Pro551=
|
|
NM_001354729.2:c.2214A>G
|
NP_001341658.1:p.Pro738=
|
|
NM_001354730.2:c.1986A>G
|
NP_001341659.1:p.Pro662=
|
|