ENST00000375128.5:c.674-262C>T
MANE Select
|
ENSP00000364270.5:n.674-262C>T
|
|
ENST00000375128.4:c.674-262C>T
|
ENSP00000364270.4:n.674-262C>T
|
|
ENST00000462523.5:c.*110-262C>T
|
ENSP00000433006.1:n.*110-262C>T
|
|
ENST00000485042.1:n.107C>T
|
|
|
NM_000380.3:c.674-262C>T , LRG_471t1:c.674-262C>T
|
NP_000371.1:n.674-262C>T
|
|
NR_027302.1:n.1022-262C>T
|
|
|
XM_006717278.1:c.674-262C>T
|
XP_006717341.1:n.674-262C>T
|
|
XM_011518988.1:c.674-262C>T
|
XP_011517290.1:n.674-262C>T
|
|
XR_929839.1:n.1126C>T
|
|
|
NM_001354975.1:c.548-262C>T
|
NP_001341904.1:n.548-262C>T
|
|
NR_149091.1:n.519-262C>T
|
|
|
NR_149092.1:n.685-262C>T
|
|
|
NR_149093.1:n.1132C>T
|
|
|
NR_149094.1:n.1026C>T
|
|
|
NM_000380.4:c.674-262C>T
MANE Select
|
NP_000371.1:n.674-262C>T
|
|
NM_001354975.2:c.548-262C>T
|
NP_001341904.1:n.548-262C>T
|
|
NR_027302.2:n.953-262C>T
|
|
|
NR_149091.2:n.450-262C>T
|
|
|
NR_149092.2:n.616-262C>T
|
|
|
NR_149093.2:n.1063C>T
|
|
|
NR_149094.2:n.957C>T
|
|
|