|
ENST00000308982.12:c.1553G>T
MANE Select
|
ENSP00000312618.7:p.Arg518Leu
|
|
|
ENST00000511325.2:n.1631G>T
|
|
|
|
ENST00000679399.1:c.*1724G>T
|
ENSP00000505434.1:n.*1724G>T
|
|
|
ENST00000679431.1:c.*1429G>T
|
ENSP00000506440.1:n.*1429G>T
|
|
|
ENST00000679613.1:c.1553G>T
|
ENSP00000504971.1:p.Arg518Leu
|
|
|
ENST00000679715.1:c.1184G>T
|
ENSP00000506228.1:p.Arg395Leu
|
|
|
ENST00000679824.1:c.*2859G>T
|
ENSP00000505516.1:n.*2859G>T
|
|
|
ENST00000679990.1:n.1788G>T
|
|
|
|
ENST00000680636.1:c.1553G>T
|
ENSP00000504886.1:p.Arg518Leu
|
|
|
ENST00000680638.1:n.1306G>T
|
|
|
|
ENST00000680744.1:c.*906G>T
|
ENSP00000505243.1:n.*906G>T
|
|
|
ENST00000680764.1:c.*2957G>T
|
ENSP00000505126.1:n.*2957G>T
|
|
|
ENST00000681319.1:n.2339G>T
|
|
|
|
ENST00000681367.1:c.1553G>T
|
ENSP00000505309.1:p.Arg518Leu
|
|
|
ENST00000681552.1:c.1150-3096G>T
|
ENSP00000505699.1:n.1150-3096G>T
|
|
|
ENST00000681583.1:c.1553G>T
|
ENSP00000506340.1:p.Arg518Leu
|
|
|
ENST00000681585.1:c.*172G>T
|
ENSP00000506316.1:n.*172G>T
|
|
|
ENST00000681784.1:n.1631G>T
|
|
|
|
ENST00000681886.1:c.*746G>T
|
ENSP00000506500.1:n.*746G>T
|
|
|
ENST00000308982.11:c.1553G>T
|
ENSP00000312618.7:p.Arg518Leu
|
|
|
ENST00000505867.5:c.*1353G>T
|
ENSP00000425346.1:n.*1353G>T
|
|
|
ENST00000508971.1:c.842G>T
|
ENSP00000422683.1:p.Arg281Leu
|
|
|
ENST00000511227.5:c.*1447G>T
|
ENSP00000425226.1:n.*1447G>T
|
|
|
ENST00000511325.1:n.534G>T
|
|
|
|
ENST00000511526.5:n.1086G>T
|
|
|
|
NM_014049.4:c.1553G>T
|
NP_054768.2:p.Arg518Leu
|
|
|
NR_033426.1:n.1931G>T
|
|
|
|
XM_011512742.1:c.1184G>T
|
XP_011511044.1:p.Arg395Leu
|
|
|
XM_024453484.1:c.1184G>T
|
XP_024309252.1:p.Arg395Leu
|
|
|
XM_024453485.1:c.1184G>T
|
XP_024309253.1:p.Arg395Leu
|
|
|
XR_427367.3:n.1629G>T
|
|
|
|
NM_014049.5:c.1553G>T
MANE Select
|
NP_054768.2:p.Arg518Leu
|
|
|
NR_033426.2:n.1801G>T
|
|
|
