ENST00000393609.8:c.856C>G
MANE Select
|
ENSP00000377233.3:p.His286Asp
|
|
ENST00000334211.12:c.121C>G
|
ENSP00000335506.8:p.His41Asp
|
|
ENST00000359373.9:c.856C>G
|
ENSP00000352332.5:p.His286Asp
|
|
ENST00000393605.7:c.136C>G
|
ENSP00000377230.3:p.His46Asp
|
|
ENST00000393609.7:c.856C>G
|
ENSP00000377233.3:p.His286Asp
|
|
ENST00000426523.5:c.121C>G
|
ENSP00000392264.1:p.His41Asp
|
|
ENST00000429686.5:c.121C>G
|
ENSP00000403127.1:p.His41Asp
|
|
ENST00000465814.5:n.1193C>G
|
|
|
NM_001040118.2:c.856C>G
|
NP_001035207.1:p.His286Asp
|
|
NM_001135190.1:c.121C>G
|
NP_001128662.1:p.His41Asp
|
|
NM_015242.4:c.121C>G
|
NP_056057.2:p.His41Asp
|
|
NM_001369489.1:c.121C>G
|
NP_001356418.1:p.His41Asp
|
|
NR_161388.1:n.838C>G
|
|
|
NM_001040118.3:c.856C>G
MANE Select
|
NP_001035207.1:p.His286Asp
|
|
NM_001135190.2:c.121C>G
|
NP_001128662.1:p.His41Asp
|
|
NM_015242.5:c.121C>G
|
NP_056057.2:p.His41Asp
|
|