ENST00000262367.10:c.7012T>G
MANE Select
|
ENSP00000262367.5:p.Ser2338Ala
|
|
ENST00000262367.9:c.7012T>G
|
ENSP00000262367.5:p.Ser2338Ala
|
|
ENST00000382070.7:c.6898T>G
|
ENSP00000371502.3:p.Ser2300Ala
|
|
NM_001079846.1:c.6898T>G
|
NP_001073315.1:p.Ser2300Ala
|
|
NM_004380.2:c.7012T>G
|
NP_004371.2:p.Ser2338Ala
|
|
XM_005255124.3:c.6967T>G
|
XP_005255181.1:p.Ser2323Ala
|
|
XM_005255125.3:c.6595T>G
|
XP_005255182.1:p.Ser2199Ala
|
|
XM_006720848.2:c.6751T>G
|
XP_006720911.1:p.Ser2251Ala
|
|
XM_011522380.1:c.6958T>G
|
XP_011520682.1:p.Ser2320Ala
|
|
XM_011522381.1:c.6259T>G
|
XP_011520683.1:p.Ser2087Ala
|
|
XM_005255124.4:c.6967T>G
|
XP_005255181.1:p.Ser2323Ala
|
|
XM_005255125.4:c.6595T>G
|
XP_005255182.1:p.Ser2199Ala
|
|
XM_006720848.3:c.6751T>G
|
XP_006720911.1:p.Ser2251Ala
|
|
XM_011522381.2:c.6259T>G
|
XP_011520683.1:p.Ser2087Ala
|
|
XM_017022944.1:c.7006T>G
|
XP_016878433.1:p.Ser2336Ala
|
|
NM_004380.3:c.7012T>G
MANE Select
|
NP_004371.2:p.Ser2338Ala
|
|