ENST00000304895.9:c.1889C>A
MANE Select
|
ENSP00000302728.4:p.Ala630Asp
|
|
ENST00000304895.8:c.1889C>A
|
ENSP00000302728.4:p.Ala630Asp
|
|
ENST00000421103.5:c.1451C>A
|
ENSP00000391390.1:p.Ala484Asp
|
|
ENST00000430730.5:c.*1156C>A
|
ENSP00000411859.1:n.*1156C>A
|
|
ENST00000447929.5:c.*1269C>A
|
ENSP00000411262.1:n.*1269C>A
|
|
ENST00000466883.5:n.2279C>A
|
|
|
NM_000181.3:c.1889C>A
|
NP_000172.2:p.Ala630Asp
|
|
NM_001284290.1:c.1451C>A
|
NP_001271219.1:p.Ala484Asp
|
|
NM_001293104.1:c.1319C>A
|
NP_001280033.1:p.Ala440Asp
|
|
NM_001293105.1:c.1232C>A
|
NP_001280034.1:p.Ala411Asp
|
|
NR_120531.1:n.1935C>A
|
|
|
XM_005250297.3:c.1736C>A
|
XP_005250354.1:p.Ala579Asp
|
|
XM_011516113.1:c.1388C>A
|
XP_011514415.1:p.Ala463Asp
|
|
XM_011516114.1:c.1217C>A
|
XP_011514416.1:p.Ala406Asp
|
|
XM_005250297.4:c.1736C>A
|
XP_005250354.1:p.Ala579Asp
|
|
XM_011516114.2:c.1217C>A
|
XP_011514416.1:p.Ala406Asp
|
|
XM_017012091.1:c.1235C>A
|
XP_016867580.1:p.Ala412Asp
|
|
XM_017012092.1:c.1166C>A
|
XP_016867581.1:p.Ala389Asp
|
|
XM_017012093.2:c.1064C>A
|
XP_016867582.1:p.Ala355Asp
|
|
XR_001744658.2:n.1696C>A
|
|
|
XR_001744659.2:n.1809C>A
|
|
|
XR_001744660.2:n.1741C>A
|
|
|
XR_001744661.2:n.1656C>A
|
|
|
XR_927461.3:n.1894C>A
|
|
|
NM_000181.4:c.1889C>A
MANE Select
|
NP_000172.2:p.Ala630Asp
|
|
NM_001284290.2:c.1451C>A
|
NP_001271219.1:p.Ala484Asp
|
|
NM_001293104.2:c.1319C>A
|
NP_001280033.1:p.Ala440Asp
|
|
NM_001293105.2:c.1232C>A
|
NP_001280034.1:p.Ala411Asp
|
|
NR_120531.2:n.1834C>A
|
|
|