ENST00000375687.10:c.3388A>G
MANE Select
|
ENSP00000364839.4:p.Met1130Val
|
|
ENST00000646985.1:c.3205A>G
|
ENSP00000495053.1:p.Met1069Val
|
|
ENST00000647223.1:n.5741A>G
|
|
|
ENST00000651418.1:c.1869+1519A>G
|
ENSP00000499150.1:n.1869+1519A>G
|
|
ENST00000306058.9:c.3373A>G
|
ENSP00000305119.5:p.Met1125Val
|
|
ENST00000375687.8:c.3388A>G
|
ENSP00000364839.4:p.Met1130Val
|
|
ENST00000613218.4:c.3388A>G
|
ENSP00000480487.1:p.Met1130Val
|
|
ENST00000620121.4:c.3388A>G
|
ENSP00000481978.1:p.Met1130Val
|
|
NM_015338.5:c.3388A>G , LRG_630t1:c.3388A>G
|
NP_056153.2:p.Met1130Val
|
|
XM_006723727.2:c.3385A>G
|
XP_006723790.1:p.Met1129Val
|
|
XM_006723728.2:c.3358A>G
|
XP_006723791.1:p.Met1120Val
|
|
XM_006723730.2:c.3304A>G
|
XP_006723793.1:p.Met1102Val
|
|
XM_006723732.2:c.3205A>G
|
XP_006723795.1:p.Met1069Val
|
|
XM_006723733.1:c.2704A>G
|
XP_006723796.1:p.Met902Val
|
|
XM_011528647.1:c.3652A>G
|
XP_011526949.1:p.Met1218Val
|
|
XM_011528648.1:c.3649A>G
|
XP_011526950.1:p.Met1217Val
|
|
XM_011528649.1:c.3568A>G
|
XP_011526951.1:p.Met1190Val
|
|
XM_011528650.1:c.3499A>G
|
XP_011526952.1:p.Met1167Val
|
|
XM_011528651.1:c.3367A>G
|
XP_011526953.1:p.Met1123Val
|
|
XM_011528652.1:c.3304A>G
|
XP_011526954.1:p.Met1102Val
|
|
NM_001363734.1:c.3205A>G
|
NP_001350663.1:p.Met1069Val
|
|
XM_006723727.3:c.3385A>G
|
XP_006723790.1:p.Met1129Val
|
|
XM_006723728.3:c.3358A>G
|
XP_006723791.1:p.Met1120Val
|
|
XM_006723730.4:c.3304A>G
|
XP_006723793.1:p.Met1102Val
|
|
XM_011528648.3:c.3649A>G
|
XP_011526950.1:p.Met1217Val
|
|
XM_011528652.2:c.3304A>G
|
XP_011526954.1:p.Met1102Val
|
|
XM_017027704.1:c.3304A>G
|
XP_016883193.1:p.Met1102Val
|
|
XM_017027705.1:c.3304A>G
|
XP_016883194.1:p.Met1102Val
|
|
XM_017027706.1:c.3235A>G
|
XP_016883195.1:p.Met1079Val
|
|
NM_015338.6:c.3388A>G
MANE Select
|
NP_056153.2:p.Met1130Val
|
|