ENST00000525346.6:c.1166G>T
|
ENSP00000435707.3:p.Arg389Met
|
|
ENST00000526780.6:c.1166G>T
|
ENSP00000435668.2:p.Arg389Met
|
|
ENST00000527316.6:c.992G>T
|
ENSP00000435047.2:p.Arg331Met
|
|
ENST00000682708.1:c.1217G>T
|
ENSP00000506866.1:p.Arg406Met
|
|
ENST00000683287.1:c.1202G>T
|
ENSP00000507607.1:p.Arg401Met
|
|
ENST00000683714.1:c.1174G>T
|
ENSP00000508207.1:p.Gly392Cys
|
|
ENST00000684396.1:n.1206G>T
|
|
|
ENST00000685320.1:c.581G>T
|
ENSP00000509319.1:p.Arg194Met
|
|
ENST00000690257.1:c.1070G>T
|
ENSP00000510750.1:p.Arg357Met
|
|
ENST00000355527.8:c.1166G>T
MANE Select
|
ENSP00000347717.4:p.Arg389Met
|
|
ENST00000355527.7:c.1166G>T
|
ENSP00000347717.3:p.Arg389Met
|
|
ENST00000407721.6:c.1166G>T
|
ENSP00000384739.2:p.Arg389Met
|
|
ENST00000525137.1:c.667G>T
|
ENSP00000435956.1:p.Gly223Cys
|
|
ENST00000533800.5:c.416G>T
|
ENSP00000435011.1:p.Arg139Met
|
|
ENST00000534795.5:c.319+2175G>T
|
|
|
NM_001163817.1:c.1166G>T
|
NP_001157289.1:p.Arg389Met
|
|
NM_001360.2:c.1166G>T , LRG_340t1:c.1166G>T
|
NP_001351.2:p.Arg389Met
|
|
XM_011544777.1:c.1300G>T
|
XP_011543079.1:p.Gly434Cys
|
|
XM_011544777.2:c.1300G>T
|
XP_011543079.1:p.Gly434Cys
|
|
NM_001163817.2:c.1166G>T
|
NP_001157289.1:p.Arg389Met
|
|
NM_001360.3:c.1166G>T
MANE Select
|
NP_001351.2:p.Arg389Met
|
|