ENST00000257904.11:c.513T>A
MANE Select
|
ENSP00000257904.5:p.Leu171=
|
|
ENST00000257904.10:c.513T>A
|
ENSP00000257904.5:p.Leu171=
|
|
ENST00000312990.10:c.265-261T>A
|
ENSP00000316889.6:n.265-261T>A
|
|
ENST00000546489.5:c.291T>A
|
ENSP00000447779.1:p.Leu97=
|
|
ENST00000547281.5:c.291T>A
|
ENSP00000447274.1:p.Leu97=
|
|
ENST00000549606.5:c.-158+1243T>A
|
ENSP00000447005.1:n.-158+1243T>A
|
|
ENST00000550419.5:c.513T>A
|
ENSP00000448098.1:p.Leu171=
|
|
ENST00000551706.1:n.879T>A
|
|
|
ENST00000551800.5:c.291T>A
|
ENSP00000449391.1:p.Leu97=
|
|
ENST00000551888.5:n.443-261T>A
|
|
|
ENST00000552254.5:c.513T>A
|
ENSP00000449179.1:p.Leu171=
|
|
ENST00000553237.5:c.*152T>A
|
ENSP00000448885.1:n.*152T>A
|
|
NM_000075.3:c.513T>A
|
NP_000066.1:p.Leu171=
|
|
NM_000075.4:c.513T>A
MANE Select
|
NP_000066.1:p.Leu171=
|
|