ENST00000375128.5:c.716C>T
MANE Select
|
ENSP00000364270.5:p.Thr239Met
|
|
ENST00000375128.4:c.716C>T
|
ENSP00000364270.4:p.Thr239Met
|
|
ENST00000462523.5:c.*152C>T
|
ENSP00000433006.1:n.*152C>T
|
|
ENST00000485042.1:n.228C>T
|
|
|
NM_000380.3:c.716C>T , LRG_471t1:c.716C>T
|
NP_000371.1:p.Thr239Met
|
|
NR_027302.1:n.1064C>T
|
|
|
XM_006717278.1:c.716C>T
|
XP_006717341.1:p.Thr239Met
|
|
XM_011518988.1:c.716C>T
|
XP_011517290.1:p.Thr239Met
|
|
XR_929839.1:n.1247C>T
|
|
|
NM_001354975.1:c.590C>T
|
NP_001341904.1:p.Thr197Met
|
|
NR_149091.1:n.561C>T
|
|
|
NR_149092.1:n.727C>T
|
|
|
NR_149093.1:n.1253C>T
|
|
|
NR_149094.1:n.1147C>T
|
|
|
NM_000380.4:c.716C>T
MANE Select
|
NP_000371.1:p.Thr239Met
|
|
NM_001354975.2:c.590C>T
|
NP_001341904.1:p.Thr197Met
|
|
NR_027302.2:n.995C>T
|
|
|
NR_149091.2:n.492C>T
|
|
|
NR_149092.2:n.658C>T
|
|
|
NR_149093.2:n.1184C>T
|
|
|
NR_149094.2:n.1078C>T
|
|
|