ENST00000375128.5:c.674-179G>T
MANE Select
|
ENSP00000364270.5:n.674-179G>T
|
|
ENST00000375128.4:c.674-179G>T
|
ENSP00000364270.4:n.674-179G>T
|
|
ENST00000462523.5:c.*110-179G>T
|
ENSP00000433006.1:n.*110-179G>T
|
|
ENST00000485042.1:n.185+5G>T
|
|
|
NM_000380.3:c.674-179G>T , LRG_471t1:c.674-179G>T
|
NP_000371.1:n.674-179G>T
|
|
NR_027302.1:n.1022-179G>T
|
|
|
XM_006717278.1:c.674-179G>T
|
XP_006717341.1:n.674-179G>T
|
|
XM_011518988.1:c.674-179G>T
|
XP_011517290.1:n.674-179G>T
|
|
XR_929839.1:n.1204+5G>T
|
|
|
NM_001354975.1:c.548-179G>T
|
NP_001341904.1:n.548-179G>T
|
|
NR_149091.1:n.519-179G>T
|
|
|
NR_149092.1:n.685-179G>T
|
|
|
NR_149093.1:n.1210+5G>T
|
|
|
NR_149094.1:n.1104+5G>T
|
|
|
NM_000380.4:c.674-179G>T
MANE Select
|
NP_000371.1:n.674-179G>T
|
|
NM_001354975.2:c.548-179G>T
|
NP_001341904.1:n.548-179G>T
|
|
NR_027302.2:n.953-179G>T
|
|
|
NR_149091.2:n.450-179G>T
|
|
|
NR_149092.2:n.616-179G>T
|
|
|
NR_149093.2:n.1141+5G>T
|
|
|
NR_149094.2:n.1035+5G>T
|
|
|