ENST00000315757.9:c.1402C>A
MANE Select
|
ENSP00000327290.7:p.His468Asn
|
|
ENST00000315757.8:c.1402C>A
|
ENSP00000327290.7:p.His468Asn
|
|
ENST00000423218.6:c.1402C>A
|
ENSP00000403392.2:p.His468Asn
|
|
ENST00000566429.1:n.291C>A
|
|
|
ENST00000569346.5:n.381C>A
|
|
|
NM_001004439.1:c.1402C>A
|
NP_001004439.1:p.His468Asn
|
|
XM_005254228.2:c.1096C>A
|
XP_005254285.1:p.His366Asn
|
|
XM_011521363.1:c.1195C>A
|
XP_011519665.1:p.His399Asn
|
|
XM_005254228.3:c.1096C>A
|
XP_005254285.1:p.His366Asn
|
|
XM_011521363.2:c.1195C>A
|
XP_011519665.1:p.His399Asn
|
|
NM_001004439.2:c.1402C>A
MANE Select
|
NP_001004439.1:p.His468Asn
|
|