ENST00000355773.6:c.1283T>G
MANE Select
|
ENSP00000348019.5:p.Ile428Ser
|
|
ENST00000355773.5:c.1283T>G
|
ENSP00000348019.5:p.Ile428Ser
|
|
NM_012434.4:c.1283T>G
|
NP_036566.1:p.Ile428Ser
|
|
XM_005248710.2:c.1232T>G
|
XP_005248767.1:p.Ile411Ser
|
|
XM_005248711.1:c.1085T>G
|
XP_005248768.1:p.Ile362Ser
|
|
XM_011535750.1:c.1135T>G
|
XP_011534052.1:p.Ser379Ala
|
|
NM_012434.5:c.1283T>G
MANE Select
|
NP_036566.1:p.Ile428Ser
|
|
NM_001382629.1:c.1052T>G
|
NP_001369558.1:p.Ile351Ser
|
|
NM_001382630.1:c.1260-5204T>G
|
NP_001369559.1:n.1260-5204T>G
|
|
NM_001382631.1:c.1304T>G
|
NP_001369560.1:p.Ile435Ser
|
|
NM_001382632.1:c.1196T>G
|
NP_001369561.1:p.Ile399Ser
|
|
NM_001382633.1:c.1283T>G
|
NP_001369562.1:p.Ile428Ser
|
|
NM_001382634.1:c.1124T>G
|
NP_001369563.1:p.Ile375Ser
|
|
NM_001382635.1:c.1280T>G
|
NP_001369564.1:p.Ile427Ser
|
|
NM_001382636.1:c.965T>G
|
NP_001369565.1:p.Ile322Ser
|
|