ENST00000375128.5:c.712G>A
MANE Select
|
ENSP00000364270.5:p.Glu238Lys
|
|
ENST00000375128.4:c.712G>A
|
ENSP00000364270.4:p.Glu238Lys
|
|
ENST00000462523.5:c.*148G>A
|
ENSP00000433006.1:n.*148G>A
|
|
ENST00000485042.1:n.224G>A
|
|
|
NM_000380.3:c.712G>A , LRG_471t1:c.712G>A
|
NP_000371.1:p.Glu238Lys
|
|
NR_027302.1:n.1060G>A
|
|
|
XM_006717278.1:c.712G>A
|
XP_006717341.1:p.Glu238Lys
|
|
XM_011518988.1:c.712G>A
|
XP_011517290.1:p.Glu238Lys
|
|
XR_929839.1:n.1243G>A
|
|
|
NM_001354975.1:c.586G>A
|
NP_001341904.1:p.Glu196Lys
|
|
NR_149091.1:n.557G>A
|
|
|
NR_149092.1:n.723G>A
|
|
|
NR_149093.1:n.1249G>A
|
|
|
NR_149094.1:n.1143G>A
|
|
|
NM_000380.4:c.712G>A
MANE Select
|
NP_000371.1:p.Glu238Lys
|
|
NM_001354975.2:c.586G>A
|
NP_001341904.1:p.Glu196Lys
|
|
NR_027302.2:n.991G>A
|
|
|
NR_149091.2:n.488G>A
|
|
|
NR_149092.2:n.654G>A
|
|
|
NR_149093.2:n.1180G>A
|
|
|
NR_149094.2:n.1074G>A
|
|
|