ENST00000261884.8:c.952C>A
MANE Select
|
ENSP00000261884.3:p.His318Asn
|
|
ENST00000261884.7:c.952C>A
|
ENSP00000261884.3:p.His318Asn
|
|
ENST00000559565.5:n.696C>A
|
|
|
ENST00000560475.1:c.20C>A
|
|
|
ENST00000560567.5:c.952C>A
|
ENSP00000453106.1:p.His318Asn
|
|
ENST00000561265.1:n.971C>A
|
|
|
NM_016213.4:c.952C>A
|
NP_057297.2:p.His318Asn
|
|
XM_005254789.1:c.262C>A
|
XP_005254846.1:p.His88Asn
|
|
XR_243130.1:n.1010C>A
|
|
|
NM_001321924.1:c.262C>A
|
NP_001308853.1:p.His88Asn
|
|
NR_135855.1:n.1012C>A
|
|
|
NM_001321924.2:c.262C>A
|
NP_001308853.1:p.His88Asn
|
|
NM_016213.5:c.952C>A
MANE Select
|
NP_057297.2:p.His318Asn
|
|
NR_135855.2:n.980C>A
|
|
|