ENST00000302850.10:c.3976A>C
MANE Select
|
ENSP00000303830.4:p.Asn1326His
|
|
ENST00000302850.9:c.3976A>C
|
ENSP00000303830.4:p.Asn1326His
|
|
ENST00000341500.9:c.3940A>C
|
ENSP00000342838.4:p.Asn1314His
|
|
NM_000208.2:c.3976A>C
|
NP_000199.2:p.Asn1326His
|
|
NM_000208.3:c.3976A>C
|
NP_000199.2:p.Asn1326His
|
|
NM_001079817.1:c.3940A>C
|
NP_001073285.1:p.Asn1314His
|
|
NM_001079817.2:c.3940A>C
|
NP_001073285.1:p.Asn1314His
|
|
XM_011527988.1:c.4051A>C
|
XP_011526290.1:p.Asn1351His
|
|
XM_011527989.1:c.4015A>C
|
XP_011526291.1:p.Asn1339His
|
|
XM_011527988.2:c.3973A>C
|
XP_011526290.2:p.Asn1325His
|
|
XM_011527989.3:c.3937A>C
|
XP_011526291.2:p.Asn1313His
|
|
NM_000208.4:c.3976A>C
MANE Select
|
NP_000199.2:p.Asn1326His
|
|
NM_001079817.3:c.3940A>C
|
NP_001073285.1:p.Asn1314His
|
|