ENST00000340855.11:c.381C>G
MANE Select
|
ENSP00000339801.6:p.Gly127=
|
|
ENST00000651111.1:c.-215-2312C>G
|
ENSP00000498395.1:n.-215-2312C>G
|
|
ENST00000340855.10:c.381C>G
|
ENSP00000339801.6:p.Gly127=
|
|
ENST00000370441.8:c.381C>G
|
ENSP00000359470.4:p.Gly127=
|
|
ENST00000422081.6:c.-215-2312C>G
|
ENSP00000477056.1:n.-215-2312C>G
|
|
ENST00000427113.2:n.770-1126C>G
|
|
|
ENST00000428056.6:c.381C>G
|
ENSP00000390241.2:p.Gly127=
|
|
ENST00000441880.1:n.114-16251C>G
|
|
|
ENST00000464251.5:c.204C>G
|
ENSP00000428980.1:p.Gly68=
|
|
ENST00000466323.5:c.381C>G
|
ENSP00000418264.1:p.Gly127=
|
|
ENST00000490775.5:n.40C>G
|
|
|
ENST00000523759.5:n.533-2312C>G
|
|
|
NM_000202.6:c.381C>G
|
NP_000193.1:p.Gly127=
|
|
NM_001166550.2:c.111C>G
|
NP_001160022.1:p.Gly37=
|
|
NM_006123.4:c.381C>G
|
NP_006114.1:p.Gly127=
|
|
NR_104128.1:n.598C>G
|
|
|
NM_000202.7:c.381C>G
|
NP_000193.1:p.Gly127=
|
|
NM_001166550.3:c.111C>G
|
NP_001160022.1:p.Gly37=
|
|
NM_000202.8:c.381C>G
MANE Select
|
NP_000193.1:p.Gly127=
|
|
NM_001166550.4:c.111C>G
|
NP_001160022.1:p.Gly37=
|
|
NM_006123.5:c.381C>G
|
NP_006114.1:p.Gly127=
|
|
NR_104128.2:n.550C>G
|
|
|