ENST00000399503.4:c.3010C>A
MANE Select
|
ENSP00000382423.3:p.His1004Asn
|
|
ENST00000399503.3:c.3010C>A
|
ENSP00000382423.3:p.His1004Asn
|
|
NM_005921.1:c.3010C>A
|
NP_005912.1:p.His1004Asn
|
|
XM_005248519.3:c.2632C>A
|
XP_005248576.2:p.His878Asn
|
|
XM_011543406.1:c.2755C>A
|
XP_011541708.1:p.His919Asn
|
|
XM_011543407.1:c.2731C>A
|
XP_011541709.1:p.His911Asn
|
|
XM_011543408.1:c.3010C>A
|
XP_011541710.1:p.His1004Asn
|
|
XM_017009484.1:c.2599C>A
|
XP_016864973.1:p.His867Asn
|
|
XM_017009485.1:c.2521C>A
|
XP_016864974.1:p.His841Asn
|
|
XR_001742068.2:n.3041C>A
|
|
|
NM_005921.2:c.3010C>A
MANE Select
|
NP_005912.1:p.His1004Asn
|
|