ENST00000285021.12:c.2255C>G
MANE Select
|
ENSP00000285021.8:p.Pro752Arg
|
|
ENST00000285021.11:c.2255C>G
|
ENSP00000285021.7:p.Pro752Arg
|
|
ENST00000427795.2:n.120C>G
|
|
|
ENST00000476581.6:c.*1708C>G
|
ENSP00000424548.1:n.*1708C>G
|
|
NM_004628.4:c.2255C>G , LRG_472t1:c.2255C>G
|
NP_004619.3:p.Pro752Arg
|
|
NR_027299.1:n.2235C>G
|
|
|
XM_011534092.1:c.2255C>G
|
XP_011532394.1:p.Pro752Arg
|
|
NM_001354726.1:c.1676C>G
|
NP_001341655.1:p.Pro559Arg
|
|
NM_001354727.1:c.2249C>G
|
NP_001341656.1:p.Pro750Arg
|
|
NM_001354729.1:c.2237C>G
|
NP_001341658.1:p.Pro746Arg
|
|
NM_001354730.1:c.2009C>G
|
NP_001341659.1:p.Pro670Arg
|
|
NR_148950.1:n.2198C>G
|
|
|
NR_148951.1:n.2074C>G
|
|
|
XR_001740256.2:n.2288C>G
|
|
|
XR_002959580.1:n.2288C>G
|
|
|
XR_002959581.1:n.3905C>G
|
|
|
NM_001354727.2:c.2249C>G
|
NP_001341656.1:p.Pro750Arg
|
|
NM_004628.5:c.2255C>G
MANE Select
|
NP_004619.3:p.Pro752Arg
|
|
NR_148950.2:n.2127C>G
|
|
|
NR_148951.2:n.2003C>G
|
|
|
NM_001354726.2:c.1676C>G
|
NP_001341655.1:p.Pro559Arg
|
|
NM_001354729.2:c.2237C>G
|
NP_001341658.1:p.Pro746Arg
|
|
NM_001354730.2:c.2009C>G
|
NP_001341659.1:p.Pro670Arg
|
|