|
NM_018026.4:c.710A>G
MANE Select
|
NP_060496.2:p.Asn237Ser
|
|
ENST00000320580.9:c.710A>G
MANE Select
|
ENSP00000316454.4:p.Asn237Ser
|
|
NM_018026.3:c.710A>G
|
NP_060496.2:p.Asn237Ser
|
|
ENST00000320580.8:c.710A>G
|
ENSP00000316454.4:p.Asn237Ser
|
|
ENST00000527224.1:n.834A>G
|
|
|
ENST00000527380.1:c.416A>G
|
ENSP00000432639.1:p.Asn139Ser
|
|
XM_011545162.1:c.389A>G
|
XP_011543464.1:p.Asn130Ser
|
|
XM_011545163.1:c.380A>G
|
XP_011543465.1:p.Asn127Ser
|
|
XM_011545164.1:c.371A>G
|
XP_011543466.1:p.Asn124Ser
|
|
XM_011545164.2:c.371A>G
|
XP_011543466.1:p.Asn124Ser
|
|
XR_001747924.1:n.921A>G
|
|