ENST00000264381.8:c.*83A>G
MANE Select
|
ENSP00000264381.3:n.*83A>G
|
|
ENST00000264381.7:c.*83A>G
|
ENSP00000264381.3:n.*83A>G
|
|
ENST00000479451.5:c.482A>G
|
ENSP00000418325.1:n.482A>G
|
|
ENST00000482958.1:c.*398A>G
|
ENSP00000419804.1:n.*398A>G
|
|
ENST00000497011.5:c.*282A>G
|
ENSP00000419505.1:n.*282A>G
|
|
NM_000055.2:c.*83A>G
|
NP_000046.1:n.*83A>G
|
|
XM_005247685.1:c.*83A>G
|
XP_005247742.1:n.*83A>G
|
|
NM_000055.3:c.*83A>G
|
NP_000046.1:n.*83A>G
|
|
NR_137635.1:n.534A>G
|
|
|
NR_137636.1:n.2138A>G
|
|
|
NM_000055.4:c.*83A>G
MANE Select
|
NP_000046.1:n.*83A>G
|
|
NR_137635.2:n.485A>G
|
|
|
NR_137636.2:n.2089A>G
|
|
|