ENST00000340855.11:c.1146C>G
MANE Select
|
ENSP00000339801.6:p.Asp382Glu
|
|
ENST00000651111.1:c.513C>G
|
ENSP00000498395.1:p.Asp171Glu
|
|
ENST00000340855.10:c.1146C>G
|
ENSP00000339801.6:p.Asp382Glu
|
|
ENST00000422081.6:c.513C>G
|
ENSP00000477056.1:p.Asp171Glu
|
|
ENST00000441880.1:n.253C>G
|
|
|
NM_000202.6:c.1146C>G
|
NP_000193.1:p.Asp382Glu
|
|
NM_001166550.2:c.876C>G
|
NP_001160022.1:p.Asp292Glu
|
|
NM_000202.7:c.1146C>G
|
NP_000193.1:p.Asp382Glu
|
|
NM_001166550.3:c.876C>G
|
NP_001160022.1:p.Asp292Glu
|
|
NM_000202.8:c.1146C>G
MANE Select
|
NP_000193.1:p.Asp382Glu
|
|
NM_001166550.4:c.876C>G
|
NP_001160022.1:p.Asp292Glu
|
|