ENST00000255078.8:c.1407G>C
MANE Select
|
ENSP00000255078.4:p.Arg469Ser
|
|
ENST00000536803.2:n.318G>C
|
|
|
ENST00000674955.1:c.*124G>C
|
ENSP00000502463.1:n.*124G>C
|
|
ENST00000675118.1:c.895G>C
|
|
|
ENST00000675205.1:n.172G>C
|
|
|
ENST00000675310.1:n.544G>C
|
|
|
ENST00000675615.1:c.1407G>C
|
ENSP00000502413.1:p.Arg469Ser
|
|
ENST00000675648.1:n.782G>C
|
|
|
ENST00000675997.1:n.113-994G>C
|
|
|
ENST00000676149.1:n.481G>C
|
|
|
ENST00000676173.1:n.2152G>C
|
|
|
ENST00000676228.1:c.*730G>C
|
ENSP00000502375.1:n.*730G>C
|
|
ENST00000255078.7:c.1407G>C
|
ENSP00000255078.3:p.Arg469Ser
|
|
ENST00000537458.5:n.524G>C
|
|
|
ENST00000539064.5:n.1166G>C
|
|
|
ENST00000543739.5:n.524G>C
|
|
|
NM_002180.2:c.1407G>C , LRG_250t1:c.1407G>C
|
NP_002171.2:p.Arg469Ser
|
|
XM_005273974.2:c.396G>C
|
XP_005274031.1:p.Arg132Ser
|
|
XM_005273975.2:c.279G>C
|
XP_005274032.1:p.Arg93Ser
|
|
XM_011544994.1:c.174G>C
|
XP_011543296.1:p.Arg58Ser
|
|
XR_949903.1:n.1509G>C
|
|
|
XM_005273975.3:c.279G>C
|
XP_005274032.1:p.Arg93Ser
|
|
XM_017017669.2:c.396G>C
|
XP_016873158.1:p.Arg132Ser
|
|
XM_017017670.2:c.396G>C
|
XP_016873159.1:p.Arg132Ser
|
|
XM_017017671.2:c.1407G>C
|
XP_016873160.1:p.Arg469Ser
|
|
XR_949903.3:n.1505G>C
|
|
|
NM_002180.3:c.1407G>C
MANE Select
|
NP_002171.2:p.Arg469Ser
|
|