ENST00000375687.10:c.3286A>G
MANE Select
|
ENSP00000364839.4:p.Met1096Val
|
|
ENST00000646985.1:c.3103A>G
|
ENSP00000495053.1:p.Met1035Val
|
|
ENST00000647223.1:n.5639A>G
|
|
|
ENST00000651418.1:c.1869+1417A>G
|
ENSP00000499150.1:n.1869+1417A>G
|
|
ENST00000306058.9:c.3271A>G
|
ENSP00000305119.5:p.Met1091Val
|
|
ENST00000375687.8:c.3286A>G
|
ENSP00000364839.4:p.Met1096Val
|
|
ENST00000613218.4:c.3286A>G
|
ENSP00000480487.1:p.Met1096Val
|
|
ENST00000620121.4:c.3286A>G
|
ENSP00000481978.1:p.Met1096Val
|
|
NM_015338.5:c.3286A>G , LRG_630t1:c.3286A>G
|
NP_056153.2:p.Met1096Val
|
|
XM_006723727.2:c.3283A>G
|
XP_006723790.1:p.Met1095Val
|
|
XM_006723728.2:c.3256A>G
|
XP_006723791.1:p.Met1086Val
|
|
XM_006723730.2:c.3202A>G
|
XP_006723793.1:p.Met1068Val
|
|
XM_006723732.2:c.3103A>G
|
XP_006723795.1:p.Met1035Val
|
|
XM_006723733.1:c.2602A>G
|
XP_006723796.1:p.Met868Val
|
|
XM_011528647.1:c.3550A>G
|
XP_011526949.1:p.Met1184Val
|
|
XM_011528648.1:c.3547A>G
|
XP_011526950.1:p.Met1183Val
|
|
XM_011528649.1:c.3466A>G
|
XP_011526951.1:p.Met1156Val
|
|
XM_011528650.1:c.3397A>G
|
XP_011526952.1:p.Met1133Val
|
|
XM_011528651.1:c.3265A>G
|
XP_011526953.1:p.Met1089Val
|
|
XM_011528652.1:c.3202A>G
|
XP_011526954.1:p.Met1068Val
|
|
NM_001363734.1:c.3103A>G
|
NP_001350663.1:p.Met1035Val
|
|
XM_006723727.3:c.3283A>G
|
XP_006723790.1:p.Met1095Val
|
|
XM_006723728.3:c.3256A>G
|
XP_006723791.1:p.Met1086Val
|
|
XM_006723730.4:c.3202A>G
|
XP_006723793.1:p.Met1068Val
|
|
XM_011528648.3:c.3547A>G
|
XP_011526950.1:p.Met1183Val
|
|
XM_011528652.2:c.3202A>G
|
XP_011526954.1:p.Met1068Val
|
|
XM_017027704.1:c.3202A>G
|
XP_016883193.1:p.Met1068Val
|
|
XM_017027705.1:c.3202A>G
|
XP_016883194.1:p.Met1068Val
|
|
XM_017027706.1:c.3133A>G
|
XP_016883195.1:p.Met1045Val
|
|
NM_015338.6:c.3286A>G
MANE Select
|
NP_056153.2:p.Met1096Val
|
|