ENST00000302804.12:c.591G>C
MANE Select
|
ENSP00000302898.6:p.Lys197Asn
|
|
ENST00000302804.11:c.591G>C
|
ENSP00000302898.6:p.Lys197Asn
|
|
ENST00000415300.6:c.534G>C
|
ENSP00000407162.1:p.Lys178Asn
|
|
ENST00000448930.5:c.486G>C
|
ENSP00000406798.2:p.Lys162Asn
|
|
ENST00000594599.1:c.75G>C
|
ENSP00000469894.1:p.Lys25Asn
|
|
ENST00000596375.1:c.*152G>C
|
ENSP00000470465.1:n.*152G>C
|
|
ENST00000598785.5:c.489G>C
|
ENSP00000471830.1:p.Lys163Asn
|
|
ENST00000599062.5:c.582G>C
|
ENSP00000469983.1:p.Lys194Asn
|
|
ENST00000601799.5:c.*890G>C
|
ENSP00000468918.1:n.*890G>C
|
|
NM_001015878.1:c.591G>C
|
NP_001015878.1:p.Lys197Asn
|
|
NM_001015879.1:c.534G>C
|
NP_001015879.1:p.Lys178Asn
|
|
NM_003160.2:c.489G>C
|
NP_003151.2:p.Lys163Asn
|
|
XR_430209.2:n.1485G>C
|
|
|
XR_430209.3:n.1528G>C
|
|
|
NM_001015878.2:c.591G>C
MANE Select
|
NP_001015878.1:p.Lys197Asn
|
|
NM_001015879.2:c.534G>C
|
NP_001015879.1:p.Lys178Asn
|
|
NM_003160.3:c.489G>C
|
NP_003151.2:p.Lys163Asn
|
|