ENST00000302850.10:c.3925A>T
MANE Select
|
ENSP00000303830.4:p.Asn1309Tyr
|
|
ENST00000302850.9:c.3925A>T
|
ENSP00000303830.4:p.Asn1309Tyr
|
|
ENST00000341500.9:c.3889A>T
|
ENSP00000342838.4:p.Asn1297Tyr
|
|
NM_000208.2:c.3925A>T
|
NP_000199.2:p.Asn1309Tyr
|
|
NM_000208.3:c.3925A>T
|
NP_000199.2:p.Asn1309Tyr
|
|
NM_001079817.1:c.3889A>T
|
NP_001073285.1:p.Asn1297Tyr
|
|
NM_001079817.2:c.3889A>T
|
NP_001073285.1:p.Asn1297Tyr
|
|
XM_011527988.1:c.4000A>T
|
XP_011526290.1:p.Asn1334Tyr
|
|
XM_011527989.1:c.3964A>T
|
XP_011526291.1:p.Asn1322Tyr
|
|
XM_011527988.2:c.3922A>T
|
XP_011526290.2:p.Asn1308Tyr
|
|
XM_011527989.3:c.3886A>T
|
XP_011526291.2:p.Asn1296Tyr
|
|
NM_000208.4:c.3925A>T
MANE Select
|
NP_000199.2:p.Asn1309Tyr
|
|
NM_001079817.3:c.3889A>T
|
NP_001073285.1:p.Asn1297Tyr
|
|