ENST00000304895.9:c.1955G>C
MANE Select
|
ENSP00000302728.4:p.Ter652Ser
|
|
ENST00000304895.8:c.1955G>C
|
ENSP00000302728.4:p.Ter652Ser
|
|
ENST00000421103.5:c.1517G>C
|
ENSP00000391390.1:p.Ter506Ser
|
|
ENST00000430730.5:c.*1222G>C
|
ENSP00000411859.1:n.*1222G>C
|
|
ENST00000447929.5:c.*1335G>C
|
ENSP00000411262.1:n.*1335G>C
|
|
ENST00000466883.5:n.2345G>C
|
|
|
NM_000181.3:c.1955G>C
|
NP_000172.2:p.Ter652Ser
|
|
NM_001284290.1:c.1517G>C
|
NP_001271219.1:p.Ter506Ser
|
|
NM_001293104.1:c.1385G>C
|
NP_001280033.1:p.Ter462Ser
|
|
NM_001293105.1:c.1298G>C
|
NP_001280034.1:p.Ter433Ser
|
|
NR_120531.1:n.2001G>C
|
|
|
XM_005250297.3:c.1802G>C
|
XP_005250354.1:p.Ter601Ser
|
|
XM_011516113.1:c.1454G>C
|
XP_011514415.1:p.Ter485Ser
|
|
XM_011516114.1:c.1283G>C
|
XP_011514416.1:p.Ter428Ser
|
|
XM_005250297.4:c.1802G>C
|
XP_005250354.1:p.Ter601Ser
|
|
XM_011516114.2:c.1283G>C
|
XP_011514416.1:p.Ter428Ser
|
|
XM_017012091.1:c.1301G>C
|
XP_016867580.1:p.Ter434Ser
|
|
XM_017012092.1:c.1232G>C
|
XP_016867581.1:p.Ter411Ser
|
|
XM_017012093.2:c.1130G>C
|
XP_016867582.1:p.Ter377Ser
|
|
XR_001744658.2:n.1762G>C
|
|
|
XR_001744659.2:n.1875G>C
|
|
|
XR_001744660.2:n.1807G>C
|
|
|
XR_001744661.2:n.1722G>C
|
|
|
XR_927461.3:n.1960G>C
|
|
|
NM_000181.4:c.1955G>C
MANE Select
|
NP_000172.2:p.Ter652Ser
|
|
NM_001284290.2:c.1517G>C
|
NP_001271219.1:p.Ter506Ser
|
|
NM_001293104.2:c.1385G>C
|
NP_001280033.1:p.Ter462Ser
|
|
NM_001293105.2:c.1298G>C
|
NP_001280034.1:p.Ter433Ser
|
|
NR_120531.2:n.1900G>C
|
|
|