ENST00000480775.3:c.*647G>A
|
ENSP00000485462.2:n.*647G>A
|
|
ENST00000623287.4:c.*678G>A
|
ENSP00000485437.1:n.*678G>A
|
|
ENST00000623632.4:c.944G>A
|
ENSP00000485288.2:p.Gly315Glu
|
|
ENST00000625194.4:c.1295G>A
|
ENSP00000485289.2:p.Gly432Glu
|
|
ENST00000636433.1:n.1275G>A
|
|
|
ENST00000636714.1:c.1253G>A
|
ENSP00000490946.1:p.Gly418Glu
|
|
ENST00000637666.2:c.1191+576G>A
|
ENSP00000489696.2:n.1191+576G>A
|
|
ENST00000637669.1:c.1253G>A
|
ENSP00000489728.1:p.Gly418Glu
|
|
ENST00000639722.1:c.*949G>A
|
ENSP00000492828.1:n.*949G>A
|
|
ENST00000674592.1:n.2767G>A
|
|
|
ENST00000675622.1:n.4320G>A
|
|
|
ENST00000679609.1:c.*863G>A
|
ENSP00000506592.1:n.*863G>A
|
|
ENST00000679656.1:n.1938G>A
|
|
|
ENST00000679723.1:c.1208G>A
|
ENSP00000505155.1:p.Gly403Glu
|
|
ENST00000679845.1:n.1561G>A
|
|
|
ENST00000679904.1:n.1649G>A
|
|
|
ENST00000680378.1:c.1340G>A
|
ENSP00000505556.1:p.Gly447Glu
|
|
ENST00000680444.1:c.*616G>A
|
ENSP00000505298.1:n.*616G>A
|
|
ENST00000680978.1:c.1253G>A
|
ENSP00000505244.1:p.Gly418Glu
|
|
ENST00000681003.1:n.716G>A
|
|
|
ENST00000681159.1:n.2657G>A
|
|
|
ENST00000216194.11:c.1295G>A
|
ENSP00000216194.8:p.Gly432Glu
|
|
ENST00000342312.9:c.1191+576G>A
|
ENSP00000341429.6:n.1191+576G>A
|
|
ENST00000623063.3:c.1253G>A
MANE Select
|
ENSP00000485525.1:p.Gly418Glu
|
|
ENST00000623387.1:n.384G>A
|
|
|
ENST00000625194.3:c.882G>A
|
|
|
NM_000026.2:c.1253G>A
|
NP_000017.1:p.Gly418Glu
|
|
NM_001123378.1:c.1191+576G>A
|
NP_001116850.1:n.1191+576G>A
|
|
XM_011529976.1:c.1253G>A
|
XP_011528278.1:p.Gly418Glu
|
|
XM_011529977.1:c.1253G>A
|
XP_011528279.1:p.Gly418Glu
|
|
XM_011529978.1:c.1191+576G>A
|
XP_011528280.1:n.1191+576G>A
|
|
XM_011529979.1:c.1253G>A
|
XP_011528281.1:p.Gly418Glu
|
|
XM_011529980.1:c.1191+576G>A
|
XP_011528282.1:n.1191+576G>A
|
|
XM_011529981.1:c.788G>A
|
XP_011528283.1:p.Gly263Glu
|
|
XM_011529982.1:c.422G>A
|
XP_011528284.1:p.Gly141Glu
|
|
XR_937824.1:n.1343G>A
|
|
|
XR_937825.1:n.1281+576G>A
|
|
|
NM_000026.3:c.1253G>A
|
NP_000017.1:p.Gly418Glu
|
|
NM_001123378.2:c.1191+576G>A
|
NP_001116850.1:n.1191+576G>A
|
|
NM_001317923.1:c.1061G>A
|
NP_001304852.1:p.Gly354Glu
|
|
NM_001363840.1:c.1253G>A
|
NP_001350769.1:p.Gly418Glu
|
|
NR_134256.1:n.1343G>A
|
|
|
XM_011529977.3:c.1253G>A
|
XP_011528279.1:p.Gly418Glu
|
|
XM_011529980.3:c.1191+576G>A
|
XP_011528282.1:n.1191+576G>A
|
|
XM_017028636.1:c.1208G>A
|
XP_016884125.1:p.Gly403Glu
|
|
XM_017028637.1:c.1208G>A
|
XP_016884126.1:p.Gly403Glu
|
|
XM_017028638.1:c.788G>A
|
XP_016884127.1:p.Gly263Glu
|
|
XM_017028639.2:c.788G>A
|
XP_016884128.1:p.Gly263Glu
|
|
XM_017028640.1:c.422G>A
|
XP_016884129.1:p.Gly141Glu
|
|
XM_024452166.1:c.1146+576G>A
|
XP_024307934.1:n.1146+576G>A
|
|
XR_001755176.2:n.1495G>A
|
|
|
XR_002958670.1:n.1280G>A
|
|
|
XR_937825.3:n.1279+576G>A
|
|
|
NM_000026.4:c.1253G>A
MANE Select
|
NP_000017.1:p.Gly418Glu
|
|
NM_001363840.2:c.1253G>A
|
NP_001350769.1:p.Gly418Glu
|
|
NM_001123378.3:c.1191+576G>A
|
NP_001116850.1:n.1191+576G>A
|
|
NM_001317923.2:c.1061G>A
|
NP_001304852.1:p.Gly354Glu
|
|
NM_001363840.3:c.1253G>A
|
NP_001350769.1:p.Gly418Glu
|
|
NR_134256.2:n.1343G>A
|
|
|