ENST00000466474.6:c.*1509G>A
|
ENSP00000511987.1:n.*1509G>A
|
|
ENST00000695525.1:n.3099G>A
|
|
|
ENST00000695558.1:c.3013G>A
|
ENSP00000512015.1:p.Asp1005Asn
|
|
ENST00000703224.1:c.*2256G>A
|
ENSP00000515242.1:n.*2256G>A
|
|
ENST00000359568.10:c.3013G>A
MANE Select
|
ENSP00000352572.5:p.Asp1005Asn
|
|
ENST00000359568.9:c.3013G>A
|
ENSP00000352572.5:p.Asp1005Asn
|
|
ENST00000480896.5:n.3282G>A
|
|
|
NM_001315529.1:c.2659G>A
|
NP_001302458.1:p.Asp887Asn
|
|
NM_006031.5:c.3013G>A
|
NP_006022.3:p.Asp1005Asn
|
|
XM_005261124.3:c.3013G>A
|
XP_005261181.1:p.Asp1005Asn
|
|
XM_011529593.1:c.3094G>A
|
XP_011527895.1:p.Asp1032Asn
|
|
XM_011529594.1:c.3094G>A
|
XP_011527896.1:p.Asp1032Asn
|
|
XM_005261124.5:c.3013G>A
|
XP_005261181.1:p.Asp1005Asn
|
|
XM_011529594.3:c.3094G>A
|
XP_011527896.1:p.Asp1032Asn
|
|
XM_017028362.2:c.3013G>A
|
XP_016883851.1:p.Asp1005Asn
|
|
XM_017028363.1:c.2659G>A
|
XP_016883852.1:p.Asp887Asn
|
|
XM_024452082.1:c.1897G>A
|
XP_024307850.1:p.Asp633Asn
|
|
XM_024452083.1:c.793G>A
|
XP_024307851.1:p.Asp265Asn
|
|
NM_006031.6:c.3013G>A
MANE Select
|
NP_006022.3:p.Asp1005Asn
|
|
NM_001315529.2:c.2659G>A
|
NP_001302458.1:p.Asp887Asn
|
|