ENST00000302850.10:c.3026C>T
MANE Select
|
ENSP00000303830.4:p.Ser1009Phe
|
|
ENST00000302850.9:c.3026C>T
|
ENSP00000303830.4:p.Ser1009Phe
|
|
ENST00000341500.9:c.2990C>T
|
ENSP00000342838.4:p.Ser997Phe
|
|
NM_000208.2:c.3026C>T
|
NP_000199.2:p.Ser1009Phe
|
|
NM_000208.3:c.3026C>T
|
NP_000199.2:p.Ser1009Phe
|
|
NM_001079817.1:c.2990C>T
|
NP_001073285.1:p.Ser997Phe
|
|
NM_001079817.2:c.2990C>T
|
NP_001073285.1:p.Ser997Phe
|
|
XM_011527988.1:c.3101C>T
|
XP_011526290.1:p.Ser1034Phe
|
|
XM_011527989.1:c.3065C>T
|
XP_011526291.1:p.Ser1022Phe
|
|
XM_011527988.2:c.3023C>T
|
XP_011526290.2:p.Ser1008Phe
|
|
XM_011527989.3:c.2987C>T
|
XP_011526291.2:p.Ser996Phe
|
|
NM_000208.4:c.3026C>T
MANE Select
|
NP_000199.2:p.Ser1009Phe
|
|
NM_001079817.3:c.2990C>T
|
NP_001073285.1:p.Ser997Phe
|
|