ENST00000393609.8:c.509+4952C>G
MANE Select
|
ENSP00000377233.3:n.509+4952C>G
|
|
ENST00000334211.12:c.-227+182C>G
|
ENSP00000335506.8:n.-227+182C>G
|
|
ENST00000359373.9:c.509+4952C>G
|
ENSP00000352332.5:n.509+4952C>G
|
|
ENST00000393609.7:c.509+4952C>G
|
ENSP00000377233.3:n.509+4952C>G
|
|
ENST00000426523.5:c.-227+182C>G
|
ENSP00000392264.1:n.-227+182C>G
|
|
ENST00000429686.5:c.-227+182C>G
|
ENSP00000403127.1:n.-227+182C>G
|
|
ENST00000465814.5:n.239+182C>G
|
|
|
NM_001040118.2:c.509+4952C>G
|
NP_001035207.1:n.509+4952C>G
|
|
NM_001135190.1:c.-227+182C>G
|
NP_001128662.1:n.-227+182C>G
|
|
NM_015242.4:c.-227+182C>G
|
NP_056057.2:n.-227+182C>G
|
|
NM_001369489.1:c.-227+182C>G
|
NP_001356418.1:n.-227+182C>G
|
|
NR_161388.1:n.491+182C>G
|
|
|
NM_001040118.3:c.509+4952C>G
MANE Select
|
NP_001035207.1:n.509+4952C>G
|
|
NM_001135190.2:c.-227+182C>G
|
NP_001128662.1:n.-227+182C>G
|
|
NM_015242.5:c.-227+182C>G
|
NP_056057.2:n.-227+182C>G
|
|