ENST00000255078.8:c.2100G>A
MANE Select
|
ENSP00000255078.4:p.Lys700=
|
|
ENST00000674675.1:c.344G>A
|
|
|
ENST00000674878.1:c.344G>A
|
|
|
ENST00000674955.1:c.*817G>A
|
ENSP00000502463.1:n.*817G>A
|
|
ENST00000675118.1:c.1588G>A
|
|
|
ENST00000675389.1:n.375G>A
|
|
|
ENST00000675615.1:c.2100G>A
|
ENSP00000502413.1:p.Lys700=
|
|
ENST00000675648.1:n.1475G>A
|
|
|
ENST00000675916.1:c.344G>A
|
|
|
ENST00000676173.1:n.2845G>A
|
|
|
ENST00000676182.1:c.531G>A
|
|
|
ENST00000676228.1:c.*1423G>A
|
ENSP00000502375.1:n.*1423G>A
|
|
ENST00000255078.7:c.2100G>A
|
ENSP00000255078.3:p.Lys700=
|
|
ENST00000539064.5:n.1859G>A
|
|
|
ENST00000543739.5:n.1093G>A
|
|
|
NM_002180.2:c.2100G>A , LRG_250t1:c.2100G>A
|
NP_002171.2:p.Lys700=
|
|
XM_005273974.2:c.1089G>A
|
XP_005274031.1:p.Lys363=
|
|
XM_005273975.2:c.972G>A
|
XP_005274032.1:p.Lys324=
|
|
XM_011544994.1:c.867G>A
|
XP_011543296.1:p.Lys289=
|
|
XR_949903.1:n.2202G>A
|
|
|
XM_005273975.3:c.972G>A
|
XP_005274032.1:p.Lys324=
|
|
XM_017017669.2:c.1089G>A
|
XP_016873158.1:p.Lys363=
|
|
XM_017017670.2:c.1089G>A
|
XP_016873159.1:p.Lys363=
|
|
XR_949903.3:n.2198G>A
|
|
|
NM_002180.3:c.2100G>A
MANE Select
|
NP_002171.2:p.Lys700=
|
|