ENST00000355773.6:c.892C>A
MANE Select
|
ENSP00000348019.5:p.His298Asn
|
|
ENST00000355773.5:c.892C>A
|
ENSP00000348019.5:p.His298Asn
|
|
NM_012434.4:c.892C>A
|
NP_036566.1:p.His298Asn
|
|
XM_005248710.2:c.841C>A
|
XP_005248767.1:p.His281Asn
|
|
XM_005248711.1:c.694C>A
|
XP_005248768.1:p.His232Asn
|
|
XM_011535750.1:c.892C>A
|
XP_011534052.1:p.His298Asn
|
|
NM_012434.5:c.892C>A
MANE Select
|
NP_036566.1:p.His298Asn
|
|
NM_001382629.1:c.661C>A
|
NP_001369558.1:p.His221Asn
|
|
NM_001382630.1:c.892C>A
|
NP_001369559.1:p.His298Asn
|
|
NM_001382631.1:c.913C>A
|
NP_001369560.1:p.His305Asn
|
|
NM_001382632.1:c.805C>A
|
NP_001369561.1:p.His269Asn
|
|
NM_001382633.1:c.892C>A
|
NP_001369562.1:p.His298Asn
|
|
NM_001382634.1:c.820-6443C>A
|
NP_001369563.1:n.820-6443C>A
|
|
NM_001382635.1:c.889C>A
|
NP_001369564.1:p.His297Asn
|
|
NM_001382636.1:c.574C>A
|
NP_001369565.1:p.His192Asn
|
|