ENST00000525748.6:c.1465T>G
MANE Select
|
ENSP00000434364.2:p.Ser489Ala
|
|
ENST00000298923.11:c.*762T>G
|
ENSP00000298923.7:n.*762T>G
|
|
ENST00000525748.5:c.1465T>G
|
ENSP00000434364.1:p.Ser489Ala
|
|
NM_004211.3:c.1465T>G
|
NP_004202.2:p.Ser489Ala
|
|
XM_005253225.1:c.763T>G
|
XP_005253282.1:p.Ser255Ala
|
|
XM_011520473.1:c.1465T>G
|
XP_011518775.1:p.Ser489Ala
|
|
NM_001318369.1:c.763T>G
|
NP_001305298.1:p.Ser255Ala
|
|
NM_004211.4:c.1465T>G
|
NP_004202.3:p.Ser489Ala
|
|
XM_017018544.2:c.589T>G
|
XP_016874033.1:p.Ser197Ala
|
|
XM_017018545.2:c.424T>G
|
XP_016874034.1:p.Ser142Ala
|
|
NM_001318369.2:c.763T>G
|
NP_001305298.1:p.Ser255Ala
|
|
NM_004211.5:c.1465T>G
MANE Select
|
NP_004202.4:p.Ser489Ala
|
|