ENST00000460843.6:c.1466T>G
MANE Select
|
ENSP00000417980.1:p.Leu489Arg
|
|
ENST00000629335.2:c.1466T>G
|
ENSP00000490056.1:p.Leu489Arg
|
|
ENST00000636027.1:c.1352T>G
|
ENSP00000489961.1:p.Leu451Arg
|
|
ENST00000637161.1:c.1373T>G
|
ENSP00000490328.1:p.Leu458Arg
|
|
ENST00000637261.1:c.1506T>G
|
ENSP00000490815.1:n.1506T>G
|
|
ENST00000637977.1:c.1411T>G
|
|
|
ENST00000638071.1:c.1093T>G
|
|
|
ENST00000640639.1:c.635T>G
|
ENSP00000491823.1:p.Leu212Arg
|
|
ENST00000371394.6:c.*1201T>G
|
ENSP00000485945.1:n.*1201T>G
|
|
ENST00000460843.5:c.1466T>G
|
ENSP00000417980.1:p.Leu489Arg
|
|
ENST00000462484.5:c.1466T>G
|
ENSP00000417328.1:p.Leu489Arg
|
|
ENST00000462942.3:c.323T>G
|
ENSP00000436107.1:p.Leu108Arg
|
|
ENST00000465566.2:c.158T>G
|
ENSP00000486261.1:p.Leu53Arg
|
|
ENST00000629808.2:c.559T>G
|
|
|
NM_001145527.1:c.1466T>G
|
NP_001138999.1:p.Leu489Arg
|
|
NM_024757.4:c.1466T>G
|
NP_079033.4:p.Leu489Arg
|
|
XM_005266105.3:c.1457T>G
|
XP_005266162.1:p.Leu486Arg
|
|
XM_005266110.1:c.1373T>G
|
XP_005266167.1:p.Leu458Arg
|
|
XM_006717288.2:c.1448T>G
|
XP_006717351.1:p.Leu483Arg
|
|
XM_011519021.1:c.1475T>G
|
XP_011517323.1:p.Leu492Arg
|
|
XM_011519022.1:c.1472T>G
|
XP_011517324.1:p.Leu491Arg
|
|
XM_011519023.1:c.1454T>G
|
XP_011517325.1:p.Leu485Arg
|
|
XM_011519024.1:c.1397T>G
|
XP_011517326.1:p.Leu466Arg
|
|
XM_011519025.1:c.1373T>G
|
XP_011517327.1:p.Leu458Arg
|
|
XM_011519026.1:c.1475T>G
|
XP_011517328.1:p.Leu492Arg
|
|
XM_011519027.1:c.1475T>G
|
XP_011517329.1:p.Leu492Arg
|
|
XM_011519028.1:c.1475T>G
|
XP_011517330.1:p.Leu492Arg
|
|
XM_011519033.1:c.1454T>G
|
XP_011517335.1:p.Leu485Arg
|
|
NM_001354259.1:c.1373T>G
|
NP_001341188.1:p.Leu458Arg
|
|
NM_001354263.1:c.1445T>G
|
NP_001341192.1:p.Leu482Arg
|
|
NM_001354611.1:c.1466T>G
|
NP_001341540.1:p.Leu489Arg
|
|
NM_001354612.1:c.1373T>G
|
NP_001341541.1:p.Leu458Arg
|
|
XM_005266105.5:c.1457T>G
|
XP_005266162.1:p.Leu486Arg
|
|
XM_011519021.3:c.1475T>G
|
XP_011517323.1:p.Leu492Arg
|
|
XM_011519022.3:c.1472T>G
|
XP_011517324.1:p.Leu491Arg
|
|
XM_011519023.3:c.1454T>G
|
XP_011517325.1:p.Leu485Arg
|
|
XM_017015134.1:c.1451T>G
|
XP_016870623.1:p.Leu484Arg
|
|
XM_017015136.2:c.1367T>G
|
XP_016870625.1:p.Leu456Arg
|
|
XM_017015137.1:c.1352T>G
|
XP_016870626.1:p.Leu451Arg
|
|
XM_017015138.1:c.1352T>G
|
XP_016870627.1:p.Leu451Arg
|
|
XM_024447674.1:c.1295T>G
|
XP_024303442.1:p.Leu432Arg
|
|
XM_024447675.1:c.1373T>G
|
XP_024303443.1:p.Leu458Arg
|
|
XM_024447676.1:c.590T>G
|
XP_024303444.1:p.Leu197Arg
|
|
XM_024447677.1:c.590T>G
|
XP_024303445.1:p.Leu197Arg
|
|
XM_024447678.1:c.1373T>G
|
XP_024303446.1:p.Leu458Arg
|
|
XM_024447679.1:c.1373T>G
|
XP_024303447.1:p.Leu458Arg
|
|
XM_024447680.1:c.1352T>G
|
XP_024303448.1:p.Leu451Arg
|
|
NM_024757.5:c.1466T>G
MANE Select
|
NP_079033.4:p.Leu489Arg
|
|
NM_001145527.2:c.1466T>G
|
NP_001138999.1:p.Leu489Arg
|
|
NM_001354259.2:c.1373T>G
|
NP_001341188.1:p.Leu458Arg
|
|
NM_001354263.2:c.1445T>G
|
NP_001341192.1:p.Leu482Arg
|
|
NM_001354611.2:c.1466T>G
|
NP_001341540.1:p.Leu489Arg
|
|
NM_001354612.2:c.1373T>G
|
NP_001341541.1:p.Leu458Arg
|
|