ENST00000692443.1:c.113C>G
MANE Select
|
ENSP00000509163.1:p.Ser38Ter
|
|
ENST00000419277.5:c.113C>G
|
ENSP00000393566.1:p.Ser38Ter
|
|
ENST00000453337.1:c.113C>G
|
ENSP00000390929.1:p.Ser38Ter
|
|
ENST00000463066.1:n.208C>G
|
|
|
ENST00000476642.5:n.89C>G
|
|
|
ENST00000479107.1:n.158C>G
|
|
|
NM_001242524.1:c.113C>G
|
NP_001229453.1:p.Ser38Ter
|
|
NM_001242525.1:c.113C>G
|
NP_001229454.1:p.Ser38Ter
|
|
NM_033554.3:c.113C>G
|
NP_291032.2:p.Ser38Ter
|
|
XM_011514559.1:c.113C>G
|
XP_011512861.1:p.Ser38Ter
|
|
NM_001242524.2:c.113C>G
|
NP_001229453.1:p.Ser38Ter
|
|
NM_001242525.2:c.113C>G
|
NP_001229454.1:p.Ser38Ter
|
|