ENST00000265594.9:c.1396A>C
MANE Select
|
ENSP00000265594.4:p.Asn466His
|
|
ENST00000265594.8:c.1396A>C
|
ENSP00000265594.4:p.Asn466His
|
|
ENST00000476176.5:c.1255A>C
|
ENSP00000420433.1:p.Asn419His
|
|
ENST00000492597.5:c.1069A>C
|
ENSP00000419898.1:p.Asn357His
|
|
ENST00000495767.5:c.*977A>C
|
ENSP00000419658.1:n.*977A>C
|
|
ENST00000497830.5:c.*993A>C
|
ENSP00000420088.1:n.*993A>C
|
|
ENST00000497959.5:c.1263+1610A>C
|
ENSP00000420648.1:n.1263+1610A>C
|
|
ENST00000539926.5:c.946A>C
|
ENSP00000441253.2:p.Asn316His
|
|
ENST00000610757.4:c.946A>C
|
ENSP00000480435.1:p.Asn316His
|
|
ENST00000629669.2:c.1263+1610A>C
|
ENSP00000486824.1:n.1263+1610A>C
|
|
NM_001293273.1:c.1045A>C
|
NP_001280202.1:p.Asn349His
|
|
NM_020166.4:c.1396A>C
|
NP_064551.3:p.Asn466His
|
|
NR_120639.1:n.1310A>C
|
|
|
NR_120640.1:n.2044+1610A>C
|
|
|
XM_006713702.1:c.1069A>C
|
XP_006713765.1:p.Asn357His
|
|
XM_011512992.1:c.1282A>C
|
XP_011511294.1:p.Asn428His
|
|
XM_011512993.1:c.1377+1610A>C
|
XP_011511295.1:n.1377+1610A>C
|
|
XR_241502.2:n.1524+1610A>C
|
|
|
XR_924159.1:n.1543A>C
|
|
|
NM_001363880.1:c.1069A>C
|
NP_001350809.1:p.Asn357His
|
|
XM_011512992.2:c.1282A>C
|
XP_011511294.1:p.Asn428His
|
|
XR_001740207.2:n.1519A>C
|
|
|
XR_001740208.2:n.1519A>C
|
|
|
XR_001740209.2:n.1470+1610A>C
|
|
|
XR_001740210.1:n.1349A>C
|
|
|
XR_002959553.1:n.1519A>C
|
|
|
XR_002959554.1:n.1500+1610A>C
|
|
|
XR_241502.3:n.1470+1610A>C
|
|
|
NM_020166.5:c.1396A>C
MANE Select
|
NP_064551.3:p.Asn466His
|
|
NM_001293273.2:c.1045A>C
|
NP_001280202.1:p.Asn349His
|
|
NR_120639.2:n.1219A>C
|
|
|
NR_120640.2:n.2044+1610A>C
|
|
|