ENST00000247933.9:c.784C>A
|
ENSP00000247933.4:p.His262Asn
|
|
ENST00000514224.2:c.784C>A
MANE Select
|
ENSP00000425081.2:p.His262Asn
|
|
ENST00000652070.1:n.840C>A
|
|
|
ENST00000247933.8:c.784C>A
|
ENSP00000247933.4:p.His262Asn
|
|
ENST00000502910.5:c.643C>A
|
ENSP00000422952.1:p.His215Asn
|
|
ENST00000514192.5:c.601C>A
|
ENSP00000423685.1:p.His201Asn
|
|
ENST00000514224.1:c.388C>A
|
ENSP00000425081.1:p.His130Asn
|
|
ENST00000514698.5:n.684C>A
|
|
|
NM_000203.4:c.784C>A
|
NP_000194.2:p.His262Asn
|
|
NR_110313.1:n.872C>A
|
|
|
XM_006713882.2:c.388C>A
|
XP_006713945.1:p.His130Asn
|
|
XM_011513459.1:c.643C>A
|
XP_011511761.1:p.His215Asn
|
|
XM_011513460.1:c.643C>A
|
XP_011511762.1:p.His215Asn
|
|
XM_011513461.1:c.577C>A
|
XP_011511763.1:p.His193Asn
|
|
XM_011513462.1:c.496C>A
|
XP_011511764.1:p.His166Asn
|
|
XM_011513463.1:c.496C>A
|
XP_011511765.1:p.His166Asn
|
|
XR_924947.1:n.853C>A
|
|
|
NM_000203.5:c.784C>A
MANE Select
|
NP_000194.2:p.His262Asn
|
|
NM_001363576.1:c.388C>A
|
NP_001350505.1:p.His130Asn
|
|
XM_011513461.2:c.577C>A
|
XP_011511763.1:p.His193Asn
|
|
XM_017008163.1:c.-177C>A
|
XP_016863652.1:n.-177C>A
|
|