ENST00000257904.11:c.483G>C
MANE Select
|
ENSP00000257904.5:p.Leu161=
|
|
ENST00000257904.10:c.483G>C
|
ENSP00000257904.5:p.Leu161=
|
|
ENST00000312990.10:c.265-291G>C
|
ENSP00000316889.6:n.265-291G>C
|
|
ENST00000546489.5:c.261G>C
|
ENSP00000447779.1:p.Leu87=
|
|
ENST00000547281.5:c.261G>C
|
ENSP00000447274.1:p.Leu87=
|
|
ENST00000549606.5:c.-158+1213G>C
|
ENSP00000447005.1:n.-158+1213G>C
|
|
ENST00000550419.5:c.483G>C
|
ENSP00000448098.1:p.Leu161=
|
|
ENST00000551706.1:n.849G>C
|
|
|
ENST00000551800.5:c.261G>C
|
ENSP00000449391.1:p.Leu87=
|
|
ENST00000551888.5:n.443-291G>C
|
|
|
ENST00000552254.5:c.483G>C
|
ENSP00000449179.1:p.Leu161=
|
|
ENST00000552388.1:c.483G>C
|
ENSP00000448963.1:p.Leu161=
|
|
ENST00000553237.5:c.*122G>C
|
ENSP00000448885.1:n.*122G>C
|
|
NM_000075.3:c.483G>C
|
NP_000066.1:p.Leu161=
|
|
NM_000075.4:c.483G>C
MANE Select
|
NP_000066.1:p.Leu161=
|
|