ENST00000355773.6:c.1338T>G
MANE Select
|
ENSP00000348019.5:p.Ser446Arg
|
|
ENST00000355773.5:c.1338T>G
|
ENSP00000348019.5:p.Ser446Arg
|
|
NM_012434.4:c.1338T>G
|
NP_036566.1:p.Ser446Arg
|
|
XM_005248710.2:c.1287T>G
|
XP_005248767.1:p.Ser429Arg
|
|
XM_005248711.1:c.1140T>G
|
XP_005248768.1:p.Ser380Arg
|
|
XM_011535750.1:c.1190T>G
|
XP_011534052.1:p.Val397Gly
|
|
NM_012434.5:c.1338T>G
MANE Select
|
NP_036566.1:p.Ser446Arg
|
|
NM_001382629.1:c.1107T>G
|
NP_001369558.1:p.Ser369Arg
|
|
NM_001382630.1:c.1260-5149T>G
|
NP_001369559.1:n.1260-5149T>G
|
|
NM_001382631.1:c.1359T>G
|
NP_001369560.1:p.Ser453Arg
|
|
NM_001382632.1:c.1251T>G
|
NP_001369561.1:p.Ser417Arg
|
|
NM_001382633.1:c.1338T>G
|
NP_001369562.1:p.Ser446Arg
|
|
NM_001382634.1:c.1179T>G
|
NP_001369563.1:p.Ser393Arg
|
|
NM_001382635.1:c.1335T>G
|
NP_001369564.1:p.Ser445Arg
|
|
NM_001382636.1:c.1020T>G
|
NP_001369565.1:p.Ser340Arg
|
|