ENST00000302850.10:c.4139A>G
MANE Select
|
ENSP00000303830.4:p.Asn1380Ser
|
|
ENST00000302850.9:c.4139A>G
|
ENSP00000303830.4:p.Asn1380Ser
|
|
ENST00000341500.9:c.4103A>G
|
ENSP00000342838.4:p.Asn1368Ser
|
|
NM_000208.2:c.4139A>G
|
NP_000199.2:p.Asn1380Ser
|
|
NM_000208.3:c.4139A>G
|
NP_000199.2:p.Asn1380Ser
|
|
NM_001079817.1:c.4103A>G
|
NP_001073285.1:p.Asn1368Ser
|
|
NM_001079817.2:c.4103A>G
|
NP_001073285.1:p.Asn1368Ser
|
|
XM_011527988.1:c.4214A>G
|
XP_011526290.1:p.Asn1405Ser
|
|
XM_011527989.1:c.4178A>G
|
XP_011526291.1:p.Asn1393Ser
|
|
XM_011527988.2:c.4136A>G
|
XP_011526290.2:p.Asn1379Ser
|
|
XM_011527989.3:c.4100A>G
|
XP_011526291.2:p.Asn1367Ser
|
|
NM_000208.4:c.4139A>G
MANE Select
|
NP_000199.2:p.Asn1380Ser
|
|
NM_001079817.3:c.4103A>G
|
NP_001073285.1:p.Asn1368Ser
|
|