|
NM_001754.5:c.994G>A
MANE Select
|
NP_001745.2:p.Asp332Asn
|
|
ENST00000675419.1:c.994G>A
MANE Select
|
ENSP00000501943.1:p.Asp332Asn
|
|
NM_001001890.2:c.913G>A
|
NP_001001890.1:p.Asp305Asn
|
|
NM_001001890.3:c.913G>A
|
NP_001001890.1:p.Asp305Asn
|
|
NM_001754.4:c.994G>A , LRG_482t1:c.994G>A
|
NP_001745.2:p.Asp332Asn
|
|
ENST00000300305.7:c.994G>A
|
ENSP00000300305.3:p.Asp332Asn
|
|
ENST00000344691.8:c.913G>A
|
ENSP00000340690.4:p.Asp305Asn
|
|
ENST00000399240.5:c.721G>A
|
ENSP00000382184.1:p.Asp241Asn
|
|
ENST00000437180.5:c.994G>A
|
ENSP00000409227.1:p.Asp332Asn
|
|
ENST00000482318.5:c.*584G>A
|
ENSP00000477067.1:n.*584G>A
|
|
XM_005261068.3:c.958G>A
|
XP_005261125.1:p.Asp320Asn
|
|
XM_005261069.3:c.802G>A
|
XP_005261126.1:p.Asp268Asn
|
|
XM_005261069.4:c.802G>A
|
XP_005261126.1:p.Asp268Asn
|
|
XM_011529766.1:c.994G>A
|
XP_011528068.1:p.Asp332Asn
|
|
XM_011529766.2:c.994G>A
|
XP_011528068.1:p.Asp332Asn
|
|
XM_011529767.1:c.955G>A
|
XP_011528069.1:p.Asp319Asn
|
|
XM_011529767.2:c.955G>A
|
XP_011528069.1:p.Asp319Asn
|
|
XM_011529768.1:c.763G>A
|
XP_011528070.1:p.Asp255Asn
|
|
XM_011529768.2:c.763G>A
|
XP_011528070.1:p.Asp255Asn
|
|
XM_017028487.1:c.841G>A
|
XP_016883976.1:p.Asp281Asn
|
|
XR_937576.1:n.4598G>A
|
|
|
XR_937576.2:n.4645G>A
|
|
