ENST00000375559.8:c.1216G=
MANE Select
|
ENSP00000364709.3:p.Gly406=
|
|
ENST00000375551.7:c.*207G=
|
ENSP00000364701.3:n.*207G=
|
|
ENST00000375559.7:c.1216G=
|
ENSP00000364709.3:p.Gly406=
|
|
ENST00000409306.5:c.*207G=
|
ENSP00000387092.1:n.*207G=
|
|
NM_000504.3:c.1216G= , LRG_548t1:c.1216G=
|
NP_000495.1:p.Gly406=
|
|
NM_001312674.1:c.1084G=
|
NP_001299603.1:p.Gly362=
|
|
NM_001312675.1:c.*207G=
|
NP_001299604.1:n.*207G=
|
|
NM_000504.4:c.1216G=
MANE Select
|
NP_000495.1:p.Gly406=
|
|
NM_001312674.2:c.1084G=
|
NP_001299603.1:p.Gly362=
|
|
NM_001312675.2:c.*207G=
|
NP_001299604.1:n.*207G=
|
|