ENST00000698238.1:c.814C>T
|
ENSP00000513620.1:p.Arg272Cys
|
|
ENST00000476941.6:c.505C>T
MANE Select
|
ENSP00000419313.1:p.Arg169Cys
|
|
ENST00000273482.10:c.403C>T
|
ENSP00000273482.6:p.Arg135Cys
|
|
ENST00000460401.1:c.243C>T
|
|
|
ENST00000476941.5:c.505C>T
|
ENSP00000419313.1:p.Arg169Cys
|
|
ENST00000612385.1:c.403C>T
|
ENSP00000481537.1:p.Arg135Cys
|
|
NM_001251845.1:c.505C>T
|
NP_001238774.1:p.Arg169Cys
|
|
NM_003304.4:c.403C>T
|
NP_003295.1:p.Arg135Cys
|
|
XM_005247738.2:c.211C>T
|
XP_005247795.1:p.Arg71Cys
|
|
XM_005247739.1:c.109C>T
|
XP_005247796.1:p.Arg37Cys
|
|
XR_241506.2:n.1033C>T
|
|
|
XR_924164.1:n.1033C>T
|
|
|
XR_924165.1:n.1033C>T
|
|
|
XR_924166.1:n.1033C>T
|
|
|
XM_005247738.4:c.211C>T
|
XP_005247795.1:p.Arg71Cys
|
|
XM_005247739.2:c.109C>T
|
XP_005247796.1:p.Arg37Cys
|
|
XM_017007121.2:c.322C>T
|
XP_016862610.1:p.Arg108Cys
|
|
XR_001740246.1:n.1164C>T
|
|
|
XR_241506.4:n.556C>T
|
|
|
NM_001251845.2:c.505C>T
MANE Select
|
NP_001238774.1:p.Arg169Cys
|
|
NM_003304.5:c.403C>T
|
NP_003295.1:p.Arg135Cys
|
|