ENST00000299314.12:c.3207T>C
MANE Select
|
ENSP00000299314.7:p.Asn1069=
|
|
ENST00000299314.11:c.3207T>C
|
ENSP00000299314.7:p.Asn1069=
|
|
ENST00000549194.1:n.73T>C
|
|
|
ENST00000550718.1:c.19T>C
|
|
|
NM_024312.4:c.3207T>C
|
NP_077288.2:p.Asn1069=
|
|
XM_006719593.2:c.3207T>C
|
XP_006719656.1:p.Asn1069=
|
|
XM_011538731.1:c.3126T>C
|
XP_011537033.1:p.Asn1042=
|
|
XM_006719593.3:c.3207T>C
|
XP_006719656.1:p.Asn1069=
|
|
XM_011538731.2:c.3126T>C
|
XP_011537033.1:p.Asn1042=
|
|
XM_017019961.1:c.2991T>C
|
XP_016875450.1:p.Asn997=
|
|
XM_017019962.2:c.1980T>C
|
XP_016875451.1:p.Asn660=
|
|
NM_024312.5:c.3207T>C
MANE Select
|
NP_077288.2:p.Asn1069=
|
|