ENST00000302850.10:c.3122A>C
MANE Select
|
ENSP00000303830.4:p.Asn1041Thr
|
|
ENST00000302850.9:c.3122A>C
|
ENSP00000303830.4:p.Asn1041Thr
|
|
ENST00000341500.9:c.3086A>C
|
ENSP00000342838.4:p.Asn1029Thr
|
|
NM_000208.2:c.3122A>C
|
NP_000199.2:p.Asn1041Thr
|
|
NM_000208.3:c.3122A>C
|
NP_000199.2:p.Asn1041Thr
|
|
NM_001079817.1:c.3086A>C
|
NP_001073285.1:p.Asn1029Thr
|
|
NM_001079817.2:c.3086A>C
|
NP_001073285.1:p.Asn1029Thr
|
|
XM_011527988.1:c.3197A>C
|
XP_011526290.1:p.Asn1066Thr
|
|
XM_011527989.1:c.3161A>C
|
XP_011526291.1:p.Asn1054Thr
|
|
XM_011527988.2:c.3119A>C
|
XP_011526290.2:p.Asn1040Thr
|
|
XM_011527989.3:c.3083A>C
|
XP_011526291.2:p.Asn1028Thr
|
|
NM_000208.4:c.3122A>C
MANE Select
|
NP_000199.2:p.Asn1041Thr
|
|
NM_001079817.3:c.3086A>C
|
NP_001073285.1:p.Asn1029Thr
|
|