ENST00000262367.10:c.4457G>T
MANE Select
|
ENSP00000262367.5:p.Cys1486Phe
|
|
ENST00000262367.9:c.4457G>T
|
ENSP00000262367.5:p.Cys1486Phe
|
|
ENST00000382070.7:c.4343G>T
|
ENSP00000371502.3:p.Cys1448Phe
|
|
ENST00000570939.2:c.3092G>T
|
ENSP00000461002.2:p.Cys1031Phe
|
|
ENST00000571763.5:n.247G>T
|
|
|
ENST00000574740.1:n.278G>T
|
|
|
ENST00000576720.1:n.3280G>T
|
|
|
NM_001079846.1:c.4343G>T
|
NP_001073315.1:p.Cys1448Phe
|
|
NM_004380.2:c.4457G>T
|
NP_004371.2:p.Cys1486Phe
|
|
XM_005255124.3:c.4412G>T
|
XP_005255181.1:p.Cys1471Phe
|
|
XM_005255125.3:c.4040G>T
|
XP_005255182.1:p.Cys1347Phe
|
|
XM_006720848.2:c.4196G>T
|
XP_006720911.1:p.Cys1399Phe
|
|
XM_011522380.1:c.4403G>T
|
XP_011520682.1:p.Cys1468Phe
|
|
XM_011522381.1:c.3704G>T
|
XP_011520683.1:p.Cys1235Phe
|
|
XM_005255124.4:c.4412G>T
|
XP_005255181.1:p.Cys1471Phe
|
|
XM_005255125.4:c.4040G>T
|
XP_005255182.1:p.Cys1347Phe
|
|
XM_006720848.3:c.4196G>T
|
XP_006720911.1:p.Cys1399Phe
|
|
XM_011522381.2:c.3704G>T
|
XP_011520683.1:p.Cys1235Phe
|
|
XM_017022944.1:c.4451G>T
|
XP_016878433.1:p.Cys1484Phe
|
|
NM_004380.3:c.4457G>T
MANE Select
|
NP_004371.2:p.Cys1486Phe
|
|