ENST00000355773.6:c.1338T>C
MANE Select
|
ENSP00000348019.5:p.Ser446=
|
|
ENST00000355773.5:c.1338T>C
|
ENSP00000348019.5:p.Ser446=
|
|
NM_012434.4:c.1338T>C
|
NP_036566.1:p.Ser446=
|
|
XM_005248710.2:c.1287T>C
|
XP_005248767.1:p.Ser429=
|
|
XM_005248711.1:c.1140T>C
|
XP_005248768.1:p.Ser380=
|
|
XM_011535750.1:c.1190T>C
|
XP_011534052.1:p.Val397Ala
|
|
NM_012434.5:c.1338T>C
MANE Select
|
NP_036566.1:p.Ser446=
|
|
NM_001382629.1:c.1107T>C
|
NP_001369558.1:p.Ser369=
|
|
NM_001382630.1:c.1260-5149T>C
|
NP_001369559.1:n.1260-5149T>C
|
|
NM_001382631.1:c.1359T>C
|
NP_001369560.1:p.Ser453=
|
|
NM_001382632.1:c.1251T>C
|
NP_001369561.1:p.Ser417=
|
|
NM_001382633.1:c.1338T>C
|
NP_001369562.1:p.Ser446=
|
|
NM_001382634.1:c.1179T>C
|
NP_001369563.1:p.Ser393=
|
|
NM_001382635.1:c.1335T>C
|
NP_001369564.1:p.Ser445=
|
|
NM_001382636.1:c.1020T>C
|
NP_001369565.1:p.Ser340=
|
|