|
ENST00000424970.7:c.874A>G
|
ENSP00000394548.3:p.Lys292Glu
|
|
|
ENST00000682227.1:c.849A>G
|
ENSP00000508363.1:p.Lys283=
|
|
|
ENST00000682243.1:c.*995A>G
|
ENSP00000507952.1:n.*995A>G
|
|
|
ENST00000682549.1:c.874A>G
|
ENSP00000507483.1:p.Lys292Glu
|
|
|
ENST00000682932.1:c.849A>G
|
ENSP00000507414.1:p.Lys283=
|
|
|
ENST00000683173.1:c.*970A>G
|
ENSP00000508032.1:n.*970A>G
|
|
|
ENST00000683221.1:c.849A>G
|
ENSP00000508093.1:p.Lys283=
|
|
|
ENST00000683401.1:n.782A>G
|
|
|
|
ENST00000683412.1:c.849A>G
|
ENSP00000507538.1:p.Lys283=
|
|
|
ENST00000683462.1:c.874A>G
|
ENSP00000507170.1:p.Lys292Glu
|
|
|
ENST00000683634.1:c.*970A>G
|
ENSP00000507087.1:n.*970A>G
|
|
|
ENST00000683706.1:c.253A>G
|
ENSP00000506745.1:p.Lys85Glu
|
|
|
ENST00000683916.1:c.874A>G
|
ENSP00000508106.1:p.Lys292Glu
|
|
|
ENST00000684289.1:c.*524A>G
|
ENSP00000506748.1:n.*524A>G
|
|
|
ENST00000684386.1:c.*63A>G
|
ENSP00000507611.1:n.*63A>G
|
|
|
ENST00000356736.5:c.849A>G
MANE Select
|
ENSP00000349174.4:p.Lys283=
|
|
|
ENST00000356736.4:c.849A>G
|
ENSP00000349174.4:p.Lys283=
|
|
|
ENST00000394833.6:c.849A>G
|
ENSP00000378310.2:p.Lys283=
|
|
|
ENST00000424970.6:c.849A>G
|
ENSP00000394548.2:p.Lys283=
|
|
|
NM_001135146.1:c.849A>G
|
NP_001128618.1:p.Lys283=
|
|
|
NM_001135147.1:c.849A>G
|
NP_001128619.1:p.Lys283=
|
|
|
NM_001135148.1:c.648A>G
|
NP_001128620.1:p.Lys216=
|
|
|
NM_022154.5:c.849A>G
|
NP_071437.3:p.Lys283=
|
|
|
XM_005263177.1:c.849A>G
|
XP_005263234.1:p.Lys283=
|
|
|
XM_011532182.1:c.207A>G
|
XP_011530484.1:p.Lys69=
|
|
|
XM_005263177.2:c.849A>G
|
XP_005263234.1:p.Lys283=
|
|
|
XM_017008541.1:c.648A>G
|
XP_016864030.1:p.Lys216=
|
|
|
XM_024454184.1:c.849A>G
|
XP_024309952.1:p.Lys283=
|
|
|
NM_001135146.2:c.849A>G
MANE Select
|
NP_001128618.1:p.Lys283=
|
|
|
NM_001135148.2:c.648A>G
|
NP_001128620.1:p.Lys216=
|
|
