ENST00000378823.8:c.2834A>G
MANE Select
|
ENSP00000368100.4:p.Asn945Ser
|
|
ENST00000638452.2:c.2537A>G
|
ENSP00000492349.2:p.Asn846Ser
|
|
ENST00000638504.1:n.2442A>G
|
|
|
ENST00000638568.2:c.2537A>G
|
ENSP00000491158.2:p.Asn846Ser
|
|
ENST00000639899.1:n.3353A>G
|
|
|
ENST00000640655.2:c.2537A>G
|
ENSP00000491596.2:p.Asn846Ser
|
|
ENST00000651160.1:c.*978A>G
|
ENSP00000498829.1:n.*978A>G
|
|
ENST00000651723.1:c.*2917A>G
|
ENSP00000498237.1:n.*2917A>G
|
|
ENST00000378823.7:c.2834A>G
|
ENSP00000368100.4:p.Asn945Ser
|
|
ENST00000423956.5:c.*1020A>G
|
ENSP00000390971.1:n.*1020A>G
|
|
ENST00000533482.5:c.*2460A>G
|
ENSP00000431225.1:n.*2460A>G
|
|
NM_005732.3:c.2834A>G
|
NP_005723.2:p.Asn945Ser
|
|
NM_005732.4:c.2834A>G
MANE Select
|
NP_005723.2:p.Asn945Ser
|
|