ENST00000375128.5:c.*76T>C
MANE Select
|
ENSP00000364270.5:n.*76T>C
|
|
ENST00000375128.4:c.*76T>C
|
ENSP00000364270.4:n.*76T>C
|
|
ENST00000462523.5:c.*334T>C
|
ENSP00000433006.1:n.*334T>C
|
|
ENST00000485042.1:n.410T>C
|
|
|
NM_000380.3:c.*76T>C , LRG_471t1:c.*76T>C
|
NP_000371.1:n.*76T>C
|
|
NR_027302.1:n.1246T>C
|
|
|
XM_006717278.1:c.772+126T>C
|
XP_006717341.1:n.772+126T>C
|
|
XM_011518988.1:c.772+126T>C
|
XP_011517290.1:n.772+126T>C
|
|
NM_001354975.1:c.*76T>C
|
NP_001341904.1:n.*76T>C
|
|
NR_149091.1:n.743T>C
|
|
|
NR_149092.1:n.909T>C
|
|
|
NR_149093.1:n.1435T>C
|
|
|
NR_149094.1:n.1329T>C
|
|
|
NM_000380.4:c.*76T>C
MANE Select
|
NP_000371.1:n.*76T>C
|
|
NM_001354975.2:c.*76T>C
|
NP_001341904.1:n.*76T>C
|
|
NR_027302.2:n.1177T>C
|
|
|
NR_149091.2:n.674T>C
|
|
|
NR_149092.2:n.840T>C
|
|
|
NR_149093.2:n.1366T>C
|
|
|
NR_149094.2:n.1260T>C
|
|
|