ENST00000375128.5:c.*48G>A
MANE Select
|
ENSP00000364270.5:n.*48G>A
|
|
ENST00000375128.4:c.*48G>A
|
ENSP00000364270.4:n.*48G>A
|
|
ENST00000462523.5:c.*306G>A
|
ENSP00000433006.1:n.*306G>A
|
|
ENST00000485042.1:n.382G>A
|
|
|
NM_000380.3:c.*48G>A , LRG_471t1:c.*48G>A
|
NP_000371.1:n.*48G>A
|
|
NR_027302.1:n.1218G>A
|
|
|
XM_006717278.1:c.772+98G>A
|
XP_006717341.1:n.772+98G>A
|
|
XM_011518988.1:c.772+98G>A
|
XP_011517290.1:n.772+98G>A
|
|
NM_001354975.1:c.*48G>A
|
NP_001341904.1:n.*48G>A
|
|
NR_149091.1:n.715G>A
|
|
|
NR_149092.1:n.881G>A
|
|
|
NR_149093.1:n.1407G>A
|
|
|
NR_149094.1:n.1301G>A
|
|
|
NM_000380.4:c.*48G>A
MANE Select
|
NP_000371.1:n.*48G>A
|
|
NM_001354975.2:c.*48G>A
|
NP_001341904.1:n.*48G>A
|
|
NR_027302.2:n.1149G>A
|
|
|
NR_149091.2:n.646G>A
|
|
|
NR_149092.2:n.812G>A
|
|
|
NR_149093.2:n.1338G>A
|
|
|
NR_149094.2:n.1232G>A
|
|
|