ENST00000355773.6:c.1340T>G
MANE Select
|
ENSP00000348019.5:p.Leu447Arg
|
|
ENST00000355773.5:c.1340T>G
|
ENSP00000348019.5:p.Leu447Arg
|
|
NM_012434.4:c.1340T>G
|
NP_036566.1:p.Leu447Arg
|
|
XM_005248710.2:c.1289T>G
|
XP_005248767.1:p.Leu430Arg
|
|
XM_005248711.1:c.1142T>G
|
XP_005248768.1:p.Leu381Arg
|
|
XM_011535750.1:c.1192T>G
|
XP_011534052.1:p.Ter398Gly
|
|
NM_012434.5:c.1340T>G
MANE Select
|
NP_036566.1:p.Leu447Arg
|
|
NM_001382629.1:c.1109T>G
|
NP_001369558.1:p.Leu370Arg
|
|
NM_001382630.1:c.1260-5147T>G
|
NP_001369559.1:n.1260-5147T>G
|
|
NM_001382631.1:c.1361T>G
|
NP_001369560.1:p.Leu454Arg
|
|
NM_001382632.1:c.1253T>G
|
NP_001369561.1:p.Leu418Arg
|
|
NM_001382633.1:c.1340T>G
|
NP_001369562.1:p.Leu447Arg
|
|
NM_001382634.1:c.1181T>G
|
NP_001369563.1:p.Leu394Arg
|
|
NM_001382635.1:c.1337T>G
|
NP_001369564.1:p.Leu446Arg
|
|
NM_001382636.1:c.1022T>G
|
NP_001369565.1:p.Leu341Arg
|
|