ENST00000255078.8:c.1520A>G
MANE Select
|
ENSP00000255078.4:p.Gln507Arg
|
|
ENST00000674955.1:c.*237A>G
|
ENSP00000502463.1:n.*237A>G
|
|
ENST00000675118.1:c.1008A>G
|
|
|
ENST00000675205.1:n.183+415A>G
|
|
|
ENST00000675615.1:c.1520A>G
|
ENSP00000502413.1:p.Gln507Arg
|
|
ENST00000675648.1:n.895A>G
|
|
|
ENST00000675997.1:n.113-568A>G
|
|
|
ENST00000676173.1:n.2265A>G
|
|
|
ENST00000676228.1:c.*843A>G
|
ENSP00000502375.1:n.*843A>G
|
|
ENST00000255078.7:c.1520A>G
|
ENSP00000255078.3:p.Gln507Arg
|
|
ENST00000537458.5:n.637A>G
|
|
|
ENST00000539064.5:n.1279A>G
|
|
|
ENST00000541229.5:n.215A>G
|
|
|
ENST00000543739.5:n.637A>G
|
|
|
NM_002180.2:c.1520A>G , LRG_250t1:c.1520A>G
|
NP_002171.2:p.Gln507Arg
|
|
XM_005273974.2:c.509A>G
|
XP_005274031.1:p.Gln170Arg
|
|
XM_005273975.2:c.392A>G
|
XP_005274032.1:p.Gln131Arg
|
|
XM_011544994.1:c.287A>G
|
XP_011543296.1:p.Gln96Arg
|
|
XR_949903.1:n.1622A>G
|
|
|
XM_005273975.3:c.392A>G
|
XP_005274032.1:p.Gln131Arg
|
|
XM_017017669.2:c.509A>G
|
XP_016873158.1:p.Gln170Arg
|
|
XM_017017670.2:c.509A>G
|
XP_016873159.1:p.Gln170Arg
|
|
XM_017017671.2:c.1520A>G
|
XP_016873160.1:p.Gln507Arg
|
|
XR_949903.3:n.1618A>G
|
|
|
NM_002180.3:c.1520A>G
MANE Select
|
NP_002171.2:p.Gln507Arg
|
|