ENST00000375128.5:c.683G>A
MANE Select
|
ENSP00000364270.5:p.Arg228Gln
|
|
ENST00000375128.4:c.683G>A
|
ENSP00000364270.4:p.Arg228Gln
|
|
ENST00000462523.5:c.*119G>A
|
ENSP00000433006.1:n.*119G>A
|
|
ENST00000485042.1:n.195G>A
|
|
|
NM_000380.3:c.683G>A , LRG_471t1:c.683G>A
|
NP_000371.1:p.Arg228Gln
|
|
NR_027302.1:n.1031G>A
|
|
|
XM_006717278.1:c.683G>A
|
XP_006717341.1:p.Arg228Gln
|
|
XM_011518988.1:c.683G>A
|
XP_011517290.1:p.Arg228Gln
|
|
XR_929839.1:n.1214G>A
|
|
|
NM_001354975.1:c.557G>A
|
NP_001341904.1:p.Arg186Gln
|
|
NR_149091.1:n.528G>A
|
|
|
NR_149092.1:n.694G>A
|
|
|
NR_149093.1:n.1220G>A
|
|
|
NR_149094.1:n.1114G>A
|
|
|
NM_000380.4:c.683G>A
MANE Select
|
NP_000371.1:p.Arg228Gln
|
|
NM_001354975.2:c.557G>A
|
NP_001341904.1:p.Arg186Gln
|
|
NR_027302.2:n.962G>A
|
|
|
NR_149091.2:n.459G>A
|
|
|
NR_149092.2:n.625G>A
|
|
|
NR_149093.2:n.1151G>A
|
|
|
NR_149094.2:n.1045G>A
|
|
|