ENST00000475778.2:n.1078C>A
|
|
|
ENST00000683214.1:n.760C>A
|
|
|
ENST00000684143.1:c.649C>A
|
ENSP00000508264.1:p.His217Asn
|
|
ENST00000684745.1:n.326C>A
|
|
|
ENST00000379374.5:c.652C>A
MANE Select
|
ENSP00000368682.4:p.His218Asn
|
|
ENST00000379374.4:c.652C>A
|
ENSP00000368682.4:p.His218Asn
|
|
NM_000444.5:c.652C>A
|
NP_000435.3:p.His218Asn
|
|
NM_001282754.1:c.652C>A
|
NP_001269683.1:p.His218Asn
|
|
XM_011545535.1:c.652C>A
|
XP_011543837.1:p.His218Asn
|
|
XM_017029579.1:c.-93-12738C>A
|
XP_016885068.1:n.-93-12738C>A
|
|
XM_024452390.1:c.361C>A
|
XP_024308158.1:p.His121Asn
|
|
XR_001755695.1:n.1331C>A
|
|
|
NM_000444.6:c.652C>A
MANE Select
|
NP_000435.3:p.His218Asn
|
|
NM_001282754.2:c.652C>A
|
NP_001269683.1:p.His218Asn
|
|