ENST00000375559.8:c.1119G>T
MANE Select
|
ENSP00000364709.3:p.Gln373His
|
|
ENST00000375551.7:c.*110G>T
|
ENSP00000364701.3:n.*110G>T
|
|
ENST00000375559.7:c.1119G>T
|
ENSP00000364709.3:p.Gln373His
|
|
ENST00000409306.5:c.*110G>T
|
ENSP00000387092.1:n.*110G>T
|
|
NM_000504.3:c.1119G>T , LRG_548t1:c.1119G>T
|
NP_000495.1:p.Gln373His
|
|
NM_001312674.1:c.987G>T
|
NP_001299603.1:p.Gln329His
|
|
NM_001312675.1:c.*110G>T
|
NP_001299604.1:n.*110G>T
|
|
NM_000504.4:c.1119G>T
MANE Select
|
NP_000495.1:p.Gln373His
|
|
NM_001312674.2:c.987G>T
|
NP_001299603.1:p.Gln329His
|
|
NM_001312675.2:c.*110G>T
|
NP_001299604.1:n.*110G>T
|
|