ENST00000302804.12:c.588G>C
MANE Select
|
ENSP00000302898.6:p.Arg196Ser
|
|
ENST00000302804.11:c.588G>C
|
ENSP00000302898.6:p.Arg196Ser
|
|
ENST00000415300.6:c.531G>C
|
ENSP00000407162.1:p.Arg177Ser
|
|
ENST00000448930.5:c.483G>C
|
ENSP00000406798.2:p.Arg161Ser
|
|
ENST00000594599.1:c.72G>C
|
ENSP00000469894.1:p.Arg24Ser
|
|
ENST00000596375.1:c.*149G>C
|
ENSP00000470465.1:n.*149G>C
|
|
ENST00000598785.5:c.486G>C
|
ENSP00000471830.1:p.Arg162Ser
|
|
ENST00000599062.5:c.579G>C
|
ENSP00000469983.1:p.Arg193Ser
|
|
ENST00000601799.5:c.*887G>C
|
ENSP00000468918.1:n.*887G>C
|
|
NM_001015878.1:c.588G>C
|
NP_001015878.1:p.Arg196Ser
|
|
NM_001015879.1:c.531G>C
|
NP_001015879.1:p.Arg177Ser
|
|
NM_003160.2:c.486G>C
|
NP_003151.2:p.Arg162Ser
|
|
XR_430209.2:n.1482G>C
|
|
|
XR_430209.3:n.1525G>C
|
|
|
NM_001015878.2:c.588G>C
MANE Select
|
NP_001015878.1:p.Arg196Ser
|
|
NM_001015879.2:c.531G>C
|
NP_001015879.1:p.Arg177Ser
|
|
NM_003160.3:c.486G>C
|
NP_003151.2:p.Arg162Ser
|
|