|
ENST00000308982.12:c.1518C>G
MANE Select
|
ENSP00000312618.7:p.Tyr506Ter
|
|
|
ENST00000511325.2:n.1596C>G
|
|
|
|
ENST00000679399.1:c.*1689C>G
|
ENSP00000505434.1:n.*1689C>G
|
|
|
ENST00000679431.1:c.*1394C>G
|
ENSP00000506440.1:n.*1394C>G
|
|
|
ENST00000679613.1:c.1518C>G
|
ENSP00000504971.1:p.Tyr506Ter
|
|
|
ENST00000679715.1:c.1149C>G
|
ENSP00000506228.1:p.Tyr383Ter
|
|
|
ENST00000679824.1:c.*2824C>G
|
ENSP00000505516.1:n.*2824C>G
|
|
|
ENST00000679990.1:n.1753C>G
|
|
|
|
ENST00000680636.1:c.1518C>G
|
ENSP00000504886.1:p.Tyr506Ter
|
|
|
ENST00000680638.1:n.1271C>G
|
|
|
|
ENST00000680744.1:c.*871C>G
|
ENSP00000505243.1:n.*871C>G
|
|
|
ENST00000680764.1:c.*2922C>G
|
ENSP00000505126.1:n.*2922C>G
|
|
|
ENST00000681319.1:n.2304C>G
|
|
|
|
ENST00000681367.1:c.1518C>G
|
ENSP00000505309.1:p.Tyr506Ter
|
|
|
ENST00000681552.1:c.1150-3131C>G
|
ENSP00000505699.1:n.1150-3131C>G
|
|
|
ENST00000681583.1:c.1518C>G
|
ENSP00000506340.1:p.Tyr506Ter
|
|
|
ENST00000681585.1:c.*137C>G
|
ENSP00000506316.1:n.*137C>G
|
|
|
ENST00000681784.1:n.1596C>G
|
|
|
|
ENST00000681886.1:c.*711C>G
|
ENSP00000506500.1:n.*711C>G
|
|
|
ENST00000308982.11:c.1518C>G
|
ENSP00000312618.7:p.Tyr506Ter
|
|
|
ENST00000505867.5:c.*1318C>G
|
ENSP00000425346.1:n.*1318C>G
|
|
|
ENST00000508971.1:c.807C>G
|
ENSP00000422683.1:p.Tyr269Ter
|
|
|
ENST00000511227.5:c.*1412C>G
|
ENSP00000425226.1:n.*1412C>G
|
|
|
ENST00000511325.1:n.499C>G
|
|
|
|
ENST00000511526.5:n.1051C>G
|
|
|
|
NM_014049.4:c.1518C>G
|
NP_054768.2:p.Tyr506Ter
|
|
|
NR_033426.1:n.1896C>G
|
|
|
|
XM_011512742.1:c.1149C>G
|
XP_011511044.1:p.Tyr383Ter
|
|
|
XM_024453484.1:c.1149C>G
|
XP_024309252.1:p.Tyr383Ter
|
|
|
XM_024453485.1:c.1149C>G
|
XP_024309253.1:p.Tyr383Ter
|
|
|
XR_427367.3:n.1594C>G
|
|
|
|
NM_014049.5:c.1518C>G
MANE Select
|
NP_054768.2:p.Tyr506Ter
|
|
|
NR_033426.2:n.1766C>G
|
|
|
