ENST00000315757.9:c.1418G>A
MANE Select
|
ENSP00000327290.7:p.Gly473Asp
|
|
ENST00000315757.8:c.1418G>A
|
ENSP00000327290.7:p.Gly473Asp
|
|
ENST00000423218.6:c.1418G>A
|
ENSP00000403392.2:p.Gly473Asp
|
|
ENST00000566429.1:n.307G>A
|
|
|
ENST00000569346.5:n.397G>A
|
|
|
NM_001004439.1:c.1418G>A
|
NP_001004439.1:p.Gly473Asp
|
|
XM_005254228.2:c.1112G>A
|
XP_005254285.1:p.Gly371Asp
|
|
XM_011521363.1:c.1211G>A
|
XP_011519665.1:p.Gly404Asp
|
|
XM_005254228.3:c.1112G>A
|
XP_005254285.1:p.Gly371Asp
|
|
XM_011521363.2:c.1211G>A
|
XP_011519665.1:p.Gly404Asp
|
|
NM_001004439.2:c.1418G>A
MANE Select
|
NP_001004439.1:p.Gly473Asp
|
|