ENST00000262367.10:c.4457G>C
MANE Select
|
ENSP00000262367.5:p.Cys1486Ser
|
|
ENST00000262367.9:c.4457G>C
|
ENSP00000262367.5:p.Cys1486Ser
|
|
ENST00000382070.7:c.4343G>C
|
ENSP00000371502.3:p.Cys1448Ser
|
|
ENST00000570939.2:c.3092G>C
|
ENSP00000461002.2:p.Cys1031Ser
|
|
ENST00000571763.5:n.247G>C
|
|
|
ENST00000574740.1:n.278G>C
|
|
|
ENST00000576720.1:n.3280G>C
|
|
|
NM_001079846.1:c.4343G>C
|
NP_001073315.1:p.Cys1448Ser
|
|
NM_004380.2:c.4457G>C
|
NP_004371.2:p.Cys1486Ser
|
|
XM_005255124.3:c.4412G>C
|
XP_005255181.1:p.Cys1471Ser
|
|
XM_005255125.3:c.4040G>C
|
XP_005255182.1:p.Cys1347Ser
|
|
XM_006720848.2:c.4196G>C
|
XP_006720911.1:p.Cys1399Ser
|
|
XM_011522380.1:c.4403G>C
|
XP_011520682.1:p.Cys1468Ser
|
|
XM_011522381.1:c.3704G>C
|
XP_011520683.1:p.Cys1235Ser
|
|
XM_005255124.4:c.4412G>C
|
XP_005255181.1:p.Cys1471Ser
|
|
XM_005255125.4:c.4040G>C
|
XP_005255182.1:p.Cys1347Ser
|
|
XM_006720848.3:c.4196G>C
|
XP_006720911.1:p.Cys1399Ser
|
|
XM_011522381.2:c.3704G>C
|
XP_011520683.1:p.Cys1235Ser
|
|
XM_017022944.1:c.4451G>C
|
XP_016878433.1:p.Cys1484Ser
|
|
NM_004380.3:c.4457G>C
MANE Select
|
NP_004371.2:p.Cys1486Ser
|
|