ENST00000426263.10:c.862A>G
MANE Select
|
ENSP00000416293.2:p.Asn288Asp
|
|
ENST00000674765.1:c.862A>G
|
ENSP00000501811.1:p.Asn288Asp
|
|
ENST00000675112.1:n.885A>G
|
|
|
ENST00000676254.1:n.1311A>G
|
|
|
ENST00000426263.7:c.862A>G
|
ENSP00000416293.2:p.Asn288Asp
|
|
ENST00000439722.2:c.741A>G
|
ENSP00000395521.2:n.741A>G
|
|
ENST00000475162.3:c.415+1028A>G
|
|
|
ENST00000630287.2:c.*177A>G
|
ENSP00000486694.1:n.*177A>G
|
|
NM_006516.2:c.862A>G
|
NP_006507.2:p.Asn288Asp
|
|
NM_006516.3:c.862A>G
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NP_006507.2:p.Asn288Asp
|
|
NM_006516.4:c.862A>G
MANE Select
|
NP_006507.2:p.Asn288Asp
|
|