ENST00000302850.10:c.3056C>T
MANE Select
|
ENSP00000303830.4:p.Ser1019Phe
|
|
ENST00000302850.9:c.3056C>T
|
ENSP00000303830.4:p.Ser1019Phe
|
|
ENST00000341500.9:c.3020C>T
|
ENSP00000342838.4:p.Ser1007Phe
|
|
NM_000208.2:c.3056C>T
|
NP_000199.2:p.Ser1019Phe
|
|
NM_000208.3:c.3056C>T
|
NP_000199.2:p.Ser1019Phe
|
|
NM_001079817.1:c.3020C>T
|
NP_001073285.1:p.Ser1007Phe
|
|
NM_001079817.2:c.3020C>T
|
NP_001073285.1:p.Ser1007Phe
|
|
XM_011527988.1:c.3131C>T
|
XP_011526290.1:p.Ser1044Phe
|
|
XM_011527989.1:c.3095C>T
|
XP_011526291.1:p.Ser1032Phe
|
|
XM_011527988.2:c.3053C>T
|
XP_011526290.2:p.Ser1018Phe
|
|
XM_011527989.3:c.3017C>T
|
XP_011526291.2:p.Ser1006Phe
|
|
NM_000208.4:c.3056C>T
MANE Select
|
NP_000199.2:p.Ser1019Phe
|
|
NM_001079817.3:c.3020C>T
|
NP_001073285.1:p.Ser1007Phe
|
|