ENST00000262367.10:c.4451T>C
MANE Select
|
ENSP00000262367.5:p.Phe1484Ser
|
|
ENST00000262367.9:c.4451T>C
|
ENSP00000262367.5:p.Phe1484Ser
|
|
ENST00000382070.7:c.4337T>C
|
ENSP00000371502.3:p.Phe1446Ser
|
|
ENST00000570939.2:c.3086T>C
|
ENSP00000461002.2:p.Phe1029Ser
|
|
ENST00000571763.5:n.241T>C
|
|
|
ENST00000574740.1:n.272T>C
|
|
|
ENST00000576720.1:n.3274T>C
|
|
|
NM_001079846.1:c.4337T>C
|
NP_001073315.1:p.Phe1446Ser
|
|
NM_004380.2:c.4451T>C
|
NP_004371.2:p.Phe1484Ser
|
|
XM_005255124.3:c.4406T>C
|
XP_005255181.1:p.Phe1469Ser
|
|
XM_005255125.3:c.4034T>C
|
XP_005255182.1:p.Phe1345Ser
|
|
XM_006720848.2:c.4190T>C
|
XP_006720911.1:p.Phe1397Ser
|
|
XM_011522380.1:c.4397T>C
|
XP_011520682.1:p.Phe1466Ser
|
|
XM_011522381.1:c.3698T>C
|
XP_011520683.1:p.Phe1233Ser
|
|
XM_005255124.4:c.4406T>C
|
XP_005255181.1:p.Phe1469Ser
|
|
XM_005255125.4:c.4034T>C
|
XP_005255182.1:p.Phe1345Ser
|
|
XM_006720848.3:c.4190T>C
|
XP_006720911.1:p.Phe1397Ser
|
|
XM_011522381.2:c.3698T>C
|
XP_011520683.1:p.Phe1233Ser
|
|
XM_017022944.1:c.4445T>C
|
XP_016878433.1:p.Phe1482Ser
|
|
NM_004380.3:c.4451T>C
MANE Select
|
NP_004371.2:p.Phe1484Ser
|
|