ENST00000302850.10:c.3862A>T
MANE Select
|
ENSP00000303830.4:p.Asn1288Tyr
|
|
ENST00000302850.9:c.3862A>T
|
ENSP00000303830.4:p.Asn1288Tyr
|
|
ENST00000341500.9:c.3826A>T
|
ENSP00000342838.4:p.Asn1276Tyr
|
|
NM_000208.2:c.3862A>T
|
NP_000199.2:p.Asn1288Tyr
|
|
NM_000208.3:c.3862A>T
|
NP_000199.2:p.Asn1288Tyr
|
|
NM_001079817.1:c.3826A>T
|
NP_001073285.1:p.Asn1276Tyr
|
|
NM_001079817.2:c.3826A>T
|
NP_001073285.1:p.Asn1276Tyr
|
|
XM_011527988.1:c.3937A>T
|
XP_011526290.1:p.Asn1313Tyr
|
|
XM_011527989.1:c.3901A>T
|
XP_011526291.1:p.Asn1301Tyr
|
|
XM_011527988.2:c.3859A>T
|
XP_011526290.2:p.Asn1287Tyr
|
|
XM_011527989.3:c.3823A>T
|
XP_011526291.2:p.Asn1275Tyr
|
|
NM_000208.4:c.3862A>T
MANE Select
|
NP_000199.2:p.Asn1288Tyr
|
|
NM_001079817.3:c.3826A>T
|
NP_001073285.1:p.Asn1276Tyr
|
|