ENST00000338883.9:c.3609T>C
MANE Select
|
ENSP00000345629.4:p.Asn1203=
|
|
ENST00000338883.8:c.3609T>C
|
ENSP00000345629.4:p.Asn1203=
|
|
ENST00000359173.7:c.2937T>C
|
|
|
ENST00000470101.1:n.1027T>C
|
|
|
ENST00000518578.5:n.3671T>C
|
|
|
NM_001001671.3:c.3609T>C
|
NP_001001671.3:p.Asn1203=
|
|
XM_011545507.1:c.3264T>C
|
XP_011543809.1:p.Asn1088=
|
|
XM_011545508.1:c.3177T>C
|
XP_011543810.1:p.Asn1059=
|
|
XM_011545509.1:c.2574T>C
|
XP_011543811.1:p.Asn858=
|
|
XM_011545510.1:c.2283T>C
|
XP_011543812.1:p.Asn761=
|
|
XM_011545511.1:c.1914T>C
|
XP_011543813.1:p.Asn638=
|
|
XM_011545507.3:c.3264T>C
|
XP_011543809.3:p.Asn1088=
|
|
XM_011545508.3:c.3177T>C
|
XP_011543810.3:p.Asn1059=
|
|
XM_011545510.2:c.2283T>C
|
XP_011543812.1:p.Asn761=
|
|
XM_011545511.2:c.1914T>C
|
XP_011543813.1:p.Asn638=
|
|
NM_001001671.4:c.3609T>C
MANE Select
|
NP_001001671.3:p.Asn1203=
|
|