ENST00000237596.7:c.1223G>A
MANE Select
|
ENSP00000237596.2:p.Ser408Asn
|
|
ENST00000237596.6:c.1223G>A
|
ENSP00000237596.2:p.Ser408Asn
|
|
ENST00000506367.1:n.670G>A
|
|
|
ENST00000508588.5:c.-295G>A
|
ENSP00000427131.1:n.-295G>A
|
|
NM_000297.3:c.1223G>A
|
NP_000288.1:p.Ser408Asn
|
|
XM_011532028.1:c.1095-3281G>A
|
XP_011530330.1:n.1095-3281G>A
|
|
XM_011532029.1:c.503G>A
|
XP_011530331.1:p.Ser168Asn
|
|
XM_011532030.1:c.383G>A
|
XP_011530332.1:p.Ser128Asn
|
|
XR_244632.2:n.1318G>A
|
|
|
NR_156488.1:n.1310G>A
|
|
|
XM_011532028.2:c.1095-3281G>A
|
XP_011530330.1:n.1095-3281G>A
|
|
XM_011532030.2:c.383G>A
|
XP_011530332.1:p.Ser128Asn
|
|
NM_000297.4:c.1223G>A
MANE Select
|
NP_000288.1:p.Ser408Asn
|
|
NR_156488.2:n.1322G>A
|
|
|