ENST00000375687.10:c.3671G>T
MANE Select
|
ENSP00000364839.4:p.Arg1224Met
|
|
ENST00000646985.1:c.3488G>T
|
ENSP00000495053.1:p.Arg1163Met
|
|
ENST00000647223.1:n.6024G>T
|
|
|
ENST00000651418.1:c.1869+1802G>T
|
ENSP00000499150.1:n.1869+1802G>T
|
|
ENST00000306058.9:c.3656G>T
|
ENSP00000305119.5:p.Arg1219Met
|
|
ENST00000375687.8:c.3671G>T
|
ENSP00000364839.4:p.Arg1224Met
|
|
ENST00000613218.4:c.3671G>T
|
ENSP00000480487.1:p.Arg1224Met
|
|
ENST00000620121.4:c.3671G>T
|
ENSP00000481978.1:p.Arg1224Met
|
|
NM_015338.5:c.3671G>T , LRG_630t1:c.3671G>T
|
NP_056153.2:p.Arg1224Met
|
|
XM_006723727.2:c.3668G>T
|
XP_006723790.1:p.Arg1223Met
|
|
XM_006723728.2:c.3641G>T
|
XP_006723791.1:p.Arg1214Met
|
|
XM_006723730.2:c.3587G>T
|
XP_006723793.1:p.Arg1196Met
|
|
XM_006723732.2:c.3488G>T
|
XP_006723795.1:p.Arg1163Met
|
|
XM_006723733.1:c.2987G>T
|
XP_006723796.1:p.Arg996Met
|
|
XM_011528647.1:c.3935G>T
|
XP_011526949.1:p.Arg1312Met
|
|
XM_011528648.1:c.3932G>T
|
XP_011526950.1:p.Arg1311Met
|
|
XM_011528649.1:c.3851G>T
|
XP_011526951.1:p.Arg1284Met
|
|
XM_011528650.1:c.3782G>T
|
XP_011526952.1:p.Arg1261Met
|
|
XM_011528651.1:c.3650G>T
|
XP_011526953.1:p.Arg1217Met
|
|
XM_011528652.1:c.3587G>T
|
XP_011526954.1:p.Arg1196Met
|
|
NM_001363734.1:c.3488G>T
|
NP_001350663.1:p.Arg1163Met
|
|
XM_006723727.3:c.3668G>T
|
XP_006723790.1:p.Arg1223Met
|
|
XM_006723728.3:c.3641G>T
|
XP_006723791.1:p.Arg1214Met
|
|
XM_006723730.4:c.3587G>T
|
XP_006723793.1:p.Arg1196Met
|
|
XM_011528648.3:c.3932G>T
|
XP_011526950.1:p.Arg1311Met
|
|
XM_011528652.2:c.3587G>T
|
XP_011526954.1:p.Arg1196Met
|
|
XM_017027704.1:c.3587G>T
|
XP_016883193.1:p.Arg1196Met
|
|
XM_017027705.1:c.3587G>T
|
XP_016883194.1:p.Arg1196Met
|
|
XM_017027706.1:c.3518G>T
|
XP_016883195.1:p.Arg1173Met
|
|
NM_015338.6:c.3671G>T
MANE Select
|
NP_056153.2:p.Arg1224Met
|
|