ENST00000304895.9:c.1811A>C
MANE Select
|
ENSP00000302728.4:p.Asn604Thr
|
|
ENST00000304895.8:c.1811A>C
|
ENSP00000302728.4:p.Asn604Thr
|
|
ENST00000421103.5:c.1373A>C
|
ENSP00000391390.1:p.Asn458Thr
|
|
ENST00000430730.5:c.*1078A>C
|
ENSP00000411859.1:n.*1078A>C
|
|
ENST00000447929.5:c.*1191A>C
|
ENSP00000411262.1:n.*1191A>C
|
|
ENST00000466883.5:n.2201A>C
|
|
|
NM_000181.3:c.1811A>C
|
NP_000172.2:p.Asn604Thr
|
|
NM_001284290.1:c.1373A>C
|
NP_001271219.1:p.Asn458Thr
|
|
NM_001293104.1:c.1241A>C
|
NP_001280033.1:p.Asn414Thr
|
|
NM_001293105.1:c.1154A>C
|
NP_001280034.1:p.Asn385Thr
|
|
NR_120531.1:n.1857A>C
|
|
|
XM_005250297.3:c.1658A>C
|
XP_005250354.1:p.Asn553Thr
|
|
XM_011516113.1:c.1310A>C
|
XP_011514415.1:p.Asn437Thr
|
|
XM_011516114.1:c.1139A>C
|
XP_011514416.1:p.Asn380Thr
|
|
XM_005250297.4:c.1658A>C
|
XP_005250354.1:p.Asn553Thr
|
|
XM_011516114.2:c.1139A>C
|
XP_011514416.1:p.Asn380Thr
|
|
XM_017012091.1:c.1157A>C
|
XP_016867580.1:p.Asn386Thr
|
|
XM_017012092.1:c.1088A>C
|
XP_016867581.1:p.Asn363Thr
|
|
XM_017012093.2:c.986A>C
|
XP_016867582.1:p.Asn329Thr
|
|
XR_001744658.2:n.1618A>C
|
|
|
XR_001744659.2:n.1731A>C
|
|
|
XR_001744660.2:n.1663A>C
|
|
|
XR_001744661.2:n.1578A>C
|
|
|
XR_927461.3:n.1816A>C
|
|
|
NM_000181.4:c.1811A>C
MANE Select
|
NP_000172.2:p.Asn604Thr
|
|
NM_001284290.2:c.1373A>C
|
NP_001271219.1:p.Asn458Thr
|
|
NM_001293104.2:c.1241A>C
|
NP_001280033.1:p.Asn414Thr
|
|
NM_001293105.2:c.1154A>C
|
NP_001280034.1:p.Asn385Thr
|
|
NR_120531.2:n.1756A>C
|
|
|