ENST00000302850.10:c.3017T>G
MANE Select
|
ENSP00000303830.4:p.Phe1006Cys
|
|
ENST00000302850.9:c.3017T>G
|
ENSP00000303830.4:p.Phe1006Cys
|
|
ENST00000341500.9:c.2981T>G
|
ENSP00000342838.4:p.Phe994Cys
|
|
NM_000208.2:c.3017T>G
|
NP_000199.2:p.Phe1006Cys
|
|
NM_000208.3:c.3017T>G
|
NP_000199.2:p.Phe1006Cys
|
|
NM_001079817.1:c.2981T>G
|
NP_001073285.1:p.Phe994Cys
|
|
NM_001079817.2:c.2981T>G
|
NP_001073285.1:p.Phe994Cys
|
|
XM_011527988.1:c.3092T>G
|
XP_011526290.1:p.Phe1031Cys
|
|
XM_011527989.1:c.3056T>G
|
XP_011526291.1:p.Phe1019Cys
|
|
XM_011527988.2:c.3014T>G
|
XP_011526290.2:p.Phe1005Cys
|
|
XM_011527989.3:c.2978T>G
|
XP_011526291.2:p.Phe993Cys
|
|
NM_000208.4:c.3017T>G
MANE Select
|
NP_000199.2:p.Phe1006Cys
|
|
NM_001079817.3:c.2981T>G
|
NP_001073285.1:p.Phe994Cys
|
|