ENST00000375559.8:c.1391G>C
MANE Select
|
ENSP00000364709.3:p.Arg464Thr
|
|
ENST00000375551.7:c.*382G>C
|
ENSP00000364701.3:n.*382G>C
|
|
ENST00000375559.7:c.1391G>C
|
ENSP00000364709.3:p.Arg464Thr
|
|
ENST00000409306.5:c.*382G>C
|
ENSP00000387092.1:n.*382G>C
|
|
NM_000504.3:c.1391G>C , LRG_548t1:c.1391G>C
|
NP_000495.1:p.Arg464Thr
|
|
NM_001312674.1:c.1259G>C
|
NP_001299603.1:p.Arg420Thr
|
|
NM_001312675.1:c.*382G>C
|
NP_001299604.1:n.*382G>C
|
|
NM_000504.4:c.1391G>C
MANE Select
|
NP_000495.1:p.Arg464Thr
|
|
NM_001312674.2:c.1259G>C
|
NP_001299603.1:p.Arg420Thr
|
|
NM_001312675.2:c.*382G>C
|
NP_001299604.1:n.*382G>C
|
|