ENST00000700061.1:c.660C>A
|
|
|
ENST00000700062.1:c.660C>A
|
|
|
ENST00000700065.1:n.2576C>A
|
|
|
ENST00000700066.1:c.2080C>A
|
ENSP00000514780.1:p.His694Asn
|
|
ENST00000281513.10:c.2563C>A
MANE Select
|
ENSP00000281513.5:p.His855Asn
|
|
ENST00000281513.9:c.2563C>A
|
ENSP00000281513.5:p.His855Asn
|
|
ENST00000441755.5:c.64C>A
|
ENSP00000396501.1:p.His22Asn
|
|
ENST00000442506.5:c.66C>A
|
|
|
NM_015909.3:c.2563C>A
|
NP_056993.2:p.His855Asn
|
|
NR_052013.2:n.2607C>A
|
|
|
XM_011510357.1:c.2434C>A
|
XP_011508659.1:p.His812Asn
|
|
XM_011510358.1:c.2563C>A
|
XP_011508660.1:p.His855Asn
|
|
XM_011510359.1:c.1924C>A
|
XP_011508661.1:p.His642Asn
|
|
XM_011510360.1:c.364C>A
|
XP_011508662.1:p.His122Asn
|
|
XM_011510361.1:c.355C>A
|
XP_011508663.1:p.His119Asn
|
|
XM_011510357.2:c.2434C>A
|
XP_011508659.1:p.His812Asn
|
|
XM_011510358.2:c.2563C>A
|
XP_011508660.1:p.His855Asn
|
|
XM_011510360.2:c.364C>A
|
XP_011508662.1:p.His122Asn
|
|
XM_011510361.2:c.355C>A
|
XP_011508663.1:p.His119Asn
|
|
XM_017004317.1:c.2563C>A
|
XP_016859806.1:p.His855Asn
|
|
XM_024452961.1:c.1924C>A
|
XP_024308729.1:p.His642Asn
|
|
NM_015909.4:c.2563C>A
MANE Select
|
NP_056993.2:p.His855Asn
|
|
NR_052013.3:n.2593C>A
|
|
|