ENST00000355773.6:c.1284C>G
MANE Select
|
ENSP00000348019.5:p.Ile428Met
|
|
ENST00000355773.5:c.1284C>G
|
ENSP00000348019.5:p.Ile428Met
|
|
NM_012434.4:c.1284C>G
|
NP_036566.1:p.Ile428Met
|
|
XM_005248710.2:c.1233C>G
|
XP_005248767.1:p.Ile411Met
|
|
XM_005248711.1:c.1086C>G
|
XP_005248768.1:p.Ile362Met
|
|
XM_011535750.1:c.1136C>G
|
XP_011534052.1:p.Ser379Ter
|
|
NM_012434.5:c.1284C>G
MANE Select
|
NP_036566.1:p.Ile428Met
|
|
NM_001382629.1:c.1053C>G
|
NP_001369558.1:p.Ile351Met
|
|
NM_001382630.1:c.1260-5203C>G
|
NP_001369559.1:n.1260-5203C>G
|
|
NM_001382631.1:c.1305C>G
|
NP_001369560.1:p.Ile435Met
|
|
NM_001382632.1:c.1197C>G
|
NP_001369561.1:p.Ile399Met
|
|
NM_001382633.1:c.1284C>G
|
NP_001369562.1:p.Ile428Met
|
|
NM_001382634.1:c.1125C>G
|
NP_001369563.1:p.Ile375Met
|
|
NM_001382635.1:c.1281C>G
|
NP_001369564.1:p.Ile427Met
|
|
NM_001382636.1:c.966C>G
|
NP_001369565.1:p.Ile322Met
|
|