|
NM_001303256.3:c.1396G>A
MANE Select
|
NP_001290185.1:p.Asp466Asn
|
|
ENST00000397641.8:c.1396G>A
MANE Select
|
ENSP00000380763.2:p.Asp466Asn
|
|
NM_001303256.1:c.1396G>A
|
NP_001290185.1:p.Asp466Asn
|
|
NM_001303256.2:c.1396G>A
|
NP_001290185.1:p.Asp466Asn
|
|
NM_001303257.1:c.1396G>A
|
NP_001290186.1:p.Asp466Asn
|
|
NM_001303257.2:c.1396G>A
|
NP_001290186.1:p.Asp466Asn
|
|
NM_014941.2:c.1210G>A
|
NP_055756.1:p.Asp404Asn
|
|
NM_014941.3:c.1210G>A
|
NP_055756.1:p.Asp404Asn
|
|
ENST00000215862.8:c.1210G>A
|
ENSP00000215862.4:p.Asp404Asn
|
|
ENST00000397641.7:c.1396G>A
|
ENSP00000380763.2:p.Asp466Asn
|
|
ENST00000469915.1:n.459-683G>A
|
|
|
ENST00000674576.1:n.2842G>A
|
|
|
ENST00000675601.1:n.1238G>A
|
|
|
ENST00000676215.1:n.2239G>A
|
|
|
XM_011530003.1:c.1420G>A
|
XP_011528305.1:p.Asp474Asn
|
|
XM_011530004.1:c.1411G>A
|
XP_011528306.1:p.Asp471Asn
|
|
XM_011530004.2:c.1411G>A
|
XP_011528306.1:p.Asp471Asn
|
|
XM_011530005.1:c.1420G>A
|
XP_011528307.1:p.Asp474Asn
|
|
XM_011530006.1:c.1261G>A
|
XP_011528308.1:p.Asp421Asn
|
|
XM_017028667.2:c.1411G>A
|
XP_016884156.1:p.Asp471Asn
|