ENST00000349556.5:c.761G=
|
ENSP00000230248.6:p.Arg254=
|
|
ENST00000488525.2:c.817G=
|
ENSP00000516042.1:p.Gly273=
|
|
ENST00000609590.2:n.1693G=
|
|
|
ENST00000704900.1:c.398G=
|
ENSP00000516059.1:p.Arg133=
|
|
ENST00000704901.1:c.*408G=
|
ENSP00000516060.1:n.*408G=
|
|
ENST00000704959.1:n.1086G=
|
|
|
ENST00000704982.1:n.1531G=
|
|
|
ENST00000704985.1:n.1927G=
|
|
|
ENST00000704986.1:n.1927G=
|
|
|
ENST00000705029.1:n.1652G=
|
|
|
ENST00000705059.1:n.1476G=
|
|
|
ENST00000705168.1:c.74G=
|
ENSP00000516071.1:p.Arg25=
|
|
ENST00000705169.1:c.74G=
|
ENSP00000516072.1:p.Arg25=
|
|
ENST00000705170.1:c.74G=
|
ENSP00000516073.1:p.Arg25=
|
|
ENST00000705171.1:n.866G=
|
|
|
ENST00000705173.1:c.*130G=
|
ENSP00000516075.1:n.*130G=
|
|
ENST00000705175.1:c.947G=
|
ENSP00000516077.1:p.Arg316=
|
|
ENST00000705176.1:c.1007G=
|
ENSP00000516078.1:p.Arg336=
|
|
ENST00000705177.1:c.*405G=
|
ENSP00000516079.1:n.*405G=
|
|
ENST00000705178.1:c.344G=
|
ENSP00000516080.1:p.Arg115=
|
|
ENST00000705179.1:c.539G=
|
ENSP00000516081.1:p.Arg180=
|
|
ENST00000705180.1:c.479G=
|
ENSP00000516082.1:p.Arg160=
|
|
ENST00000705235.1:c.821G=
|
ENSP00000516093.1:p.Arg274=
|
|
ENST00000705236.1:c.761G=
|
ENSP00000516094.1:p.Arg254=
|
|
ENST00000705237.1:c.479G=
|
ENSP00000516095.1:p.Arg160=
|
|
ENST00000705238.1:c.680G=
|
ENSP00000516096.1:p.Arg227=
|
|
ENST00000705239.1:c.758G=
|
ENSP00000516097.1:p.Arg253=
|
|
ENST00000705240.1:c.*430G=
|
ENSP00000516098.1:n.*430G=
|
|
ENST00000705241.1:c.757G=
|
ENSP00000516099.1:p.Gly253=
|
|
ENST00000705242.1:c.758G=
|
ENSP00000516100.1:p.Arg253=
|
|
ENST00000705249.1:c.761G=
|
ENSP00000516101.1:p.Arg254=
|
|
ENST00000705250.1:c.539G=
|
ENSP00000516102.1:p.Arg180=
|
|
ENST00000705251.1:c.*408G=
|
ENSP00000516103.1:n.*408G=
|
|
ENST00000705252.1:c.*231G=
|
ENSP00000516104.1:n.*231G=
|
|
ENST00000705253.1:c.*231G=
|
ENSP00000516105.1:n.*231G=
|
|
ENST00000705254.1:c.368G=
|
ENSP00000516106.1:p.Arg123=
|
|
ENST00000705255.1:n.1387G=
|
|
|
ENST00000705256.1:c.818G=
|
ENSP00000516107.1:p.Arg273=
|
|
ENST00000366847.9:c.821G=
MANE Select
|
ENSP00000355812.3:p.Arg274=
|
|
ENST00000349556.4:c.761G=
|
ENSP00000230248.6:p.Arg254=
|
|
ENST00000366847.8:c.821G=
|
ENSP00000355812.3:p.Arg274=
|
|
ENST00000488525.1:n.7G=
|
|
|
ENST00000496181.1:n.225G=
|
|
|
ENST00000622353.4:c.680G=
|
ENSP00000479115.1:p.Arg227=
|
|
NM_001278690.1:c.680G=
|
NP_001265619.1:p.Arg227=
|
|
NM_007045.3:c.821G=
|
NP_008976.1:p.Arg274=
|
|
NM_194429.2:c.761G=
|
NP_919410.1:p.Arg254=
|
|
NM_007045.4:c.821G=
MANE Select
|
NP_008976.1:p.Arg274=
|
|
NM_194429.3:c.761G=
|
NP_919410.1:p.Arg254=
|
|
NM_001278690.2:c.680G=
|
NP_001265619.1:p.Arg227=
|
|