ENST00000375128.5:c.777G>C
MANE Select
|
ENSP00000364270.5:p.Lys259Asn
|
|
ENST00000375128.4:c.777G>C
|
ENSP00000364270.4:p.Lys259Asn
|
|
ENST00000462523.5:c.*213G>C
|
ENSP00000433006.1:n.*213G>C
|
|
ENST00000485042.1:n.289G>C
|
|
|
NM_000380.3:c.777G>C , LRG_471t1:c.777G>C
|
NP_000371.1:p.Lys259Asn
|
|
NR_027302.1:n.1125G>C
|
|
|
XM_006717278.1:c.772+5G>C
|
XP_006717341.1:n.772+5G>C
|
|
XM_011518988.1:c.772+5G>C
|
XP_011517290.1:n.772+5G>C
|
|
NM_001354975.1:c.651G>C
|
NP_001341904.1:p.Lys217Asn
|
|
NR_149091.1:n.622G>C
|
|
|
NR_149092.1:n.788G>C
|
|
|
NR_149093.1:n.1314G>C
|
|
|
NR_149094.1:n.1208G>C
|
|
|
NM_000380.4:c.777G>C
MANE Select
|
NP_000371.1:p.Lys259Asn
|
|
NM_001354975.2:c.651G>C
|
NP_001341904.1:p.Lys217Asn
|
|
NR_027302.2:n.1056G>C
|
|
|
NR_149091.2:n.553G>C
|
|
|
NR_149092.2:n.719G>C
|
|
|
NR_149093.2:n.1245G>C
|
|
|
NR_149094.2:n.1139G>C
|
|
|