ENST00000269571.10:c.3532A>G
MANE Select
|
ENSP00000269571.4:p.Asn1178Asp
|
|
ENST00000269571.9:c.3532A>G
|
ENSP00000269571.4:p.Asn1178Asp
|
|
ENST00000406381.6:c.3442A>G
|
ENSP00000385185.2:p.Asn1148Asp
|
|
ENST00000445658.6:c.2704A>G
|
ENSP00000404047.2:p.Asn902Asp
|
|
ENST00000541774.5:c.3487A>G
|
ENSP00000446466.1:p.Asn1163Asp
|
|
ENST00000578373.5:c.*3322A>G
|
ENSP00000463427.1:n.*3322A>G
|
|
ENST00000584450.5:c.*111A>G
|
ENSP00000463714.1:n.*111A>G
|
|
ENST00000584601.5:c.3442A>G
|
ENSP00000462438.1:p.Asn1148Asp
|
|
NM_001005862.2:c.3442A>G , LRG_724t1:c.3442A>G
|
NP_001005862.1:p.Asn1148Asp
|
|
NM_001289936.1:c.3487A>G , LRG_724t4:c.3487A>G
|
NP_001276865.1:p.Asn1163Asp
|
|
NM_001289937.1:c.*111A>G
|
NP_001276866.1:n.*111A>G
|
|
NM_004448.3:c.3532A>G , LRG_724t2:c.3532A>G
|
NP_004439.2:p.Asn1178Asp
|
|
NR_110535.1:n.3856A>G
|
|
|
XM_024450641.1:c.3670A>G
|
XP_024306409.1:p.Asn1224Asp
|
|
XM_024450642.1:c.3625A>G
|
XP_024306410.1:p.Asn1209Asp
|
|
XM_024450643.1:c.3580A>G
|
XP_024306411.1:p.Asn1194Asp
|
|
NM_001005862.3:c.3442A>G
|
NP_001005862.1:p.Asn1148Asp
|
|
NM_001289936.2:c.3487A>G
|
NP_001276865.1:p.Asn1163Asp
|
|
NM_001289937.2:c.*111A>G
|
NP_001276866.1:n.*111A>G
|
|
NM_001382782.1:c.3442A>G
|
NP_001369711.1:p.Asn1148Asp
|
|
NM_001382783.1:c.3442A>G
|
NP_001369712.1:p.Asn1148Asp
|
|
NM_001382784.1:c.3649A>G
|
NP_001369713.1:p.Asn1217Asp
|
|
NM_001382785.1:c.3634A>G
|
NP_001369714.1:p.Asn1212Asp
|
|
NM_001382786.1:c.3613A>G
|
NP_001369715.1:p.Asn1205Asp
|
|
NM_001382787.1:c.3607A>G
|
NP_001369716.1:p.Asn1203Asp
|
|
NM_001382788.1:c.3562A>G
|
NP_001369717.1:p.Asn1188Asp
|
|
NM_001382789.1:c.3553A>G
|
NP_001369718.1:p.Asn1185Asp
|
|
NM_001382790.1:c.3529A>G
|
NP_001369719.1:p.Asn1177Asp
|
|
NM_001382791.1:c.3523A>G
|
NP_001369720.1:p.Asn1175Asp
|
|
NM_001382792.1:c.3496A>G
|
NP_001369721.1:p.Asn1166Asp
|
|
NM_001382793.1:c.3490A>G
|
NP_001369722.1:p.Asn1164Asp
|
|
NM_001382794.1:c.3490A>G
|
NP_001369723.1:p.Asn1164Asp
|
|
NM_001382795.1:c.3484A>G
|
NP_001369724.1:p.Asn1162Asp
|
|
NM_001382796.1:c.3445A>G
|
NP_001369725.1:p.Asn1149Asp
|
|
NM_001382797.1:c.3433A>G
|
NP_001369726.1:p.Asn1145Asp
|
|
NM_001382798.1:c.3376A>G
|
NP_001369727.1:p.Asn1126Asp
|
|
NM_001382799.1:c.3352A>G
|
NP_001369728.1:p.Asn1118Asp
|
|
NM_001382800.1:c.3346A>G
|
NP_001369729.1:p.Asn1116Asp
|
|
NM_001382801.1:c.3328A>G
|
NP_001369730.1:p.Asn1110Asp
|
|
NM_001382802.1:c.3274A>G
|
NP_001369731.1:p.Asn1092Asp
|
|
NM_001382803.1:c.*111A>G
|
NP_001369732.1:n.*111A>G
|
|
NM_001382804.1:c.2704A>G
|
NP_001369733.1:p.Asn902Asp
|
|
NM_001382805.1:c.2581A>G
|
NP_001369734.1:p.Asn861Asp
|
|
NM_001382806.1:c.2494A>G
|
NP_001369735.1:p.Asn832Asp
|
|
NM_004448.4:c.3532A>G
MANE Select
|
NP_004439.2:p.Asn1178Asp
|
|
NR_110535.2:n.3770A>G
|
|
|