ENST00000378823.8:c.2029A>G
MANE Select
|
ENSP00000368100.4:p.Asn677Asp
|
|
ENST00000638452.2:c.1732A>G
|
ENSP00000492349.2:p.Asn578Asp
|
|
ENST00000638504.1:n.1637A>G
|
|
|
ENST00000638568.2:c.1732A>G
|
ENSP00000491158.2:p.Asn578Asp
|
|
ENST00000639899.1:n.2548A>G
|
|
|
ENST00000640655.2:c.1732A>G
|
ENSP00000491596.2:p.Asn578Asp
|
|
ENST00000651160.1:c.*173A>G
|
ENSP00000498829.1:n.*173A>G
|
|
ENST00000651658.1:n.2572A>G
|
|
|
ENST00000651723.1:c.*2112A>G
|
ENSP00000498237.1:n.*2112A>G
|
|
ENST00000652016.1:c.*246A>G
|
ENSP00000498267.1:n.*246A>G
|
|
ENST00000652485.1:c.2062A>G
|
ENSP00000498973.1:p.Asn688Asp
|
|
ENST00000378823.7:c.2029A>G
|
ENSP00000368100.4:p.Asn677Asp
|
|
ENST00000423956.5:c.*215A>G
|
ENSP00000390971.1:n.*215A>G
|
|
ENST00000453394.5:c.1846A>G
|
ENSP00000400049.1:p.Asn616Asp
|
|
ENST00000496204.1:n.112A>G
|
|
|
ENST00000533482.5:c.*1655A>G
|
ENSP00000431225.1:n.*1655A>G
|
|
NM_005732.3:c.2029A>G
|
NP_005723.2:p.Asn677Asp
|
|
NM_005732.4:c.2029A>G
MANE Select
|
NP_005723.2:p.Asn677Asp
|
|