ENST00000343307.5:c.1071C>G
MANE Select
|
ENSP00000343002.4:p.Ser357=
|
|
ENST00000343307.4:c.1071C>G
|
ENSP00000343002.4:p.Ser357=
|
|
NM_194318.3:c.1071C>G
|
NP_919299.3:p.Ser357=
|
|
XM_006719768.2:c.1014C>G
|
XP_006719831.1:p.Ser338=
|
|
XM_011534936.1:c.1065-6179C>G
|
XP_011533238.1:n.1065-6179C>G
|
|
XM_011534937.1:c.951C>G
|
XP_011533239.1:p.Ser317=
|
|
XM_011534938.1:c.924C>G
|
XP_011533240.1:p.Ser308=
|
|
XR_941500.1:n.1256C>G
|
|
|
XR_941501.1:n.1136C>G
|
|
|
XM_006719768.3:c.1014C>G
|
XP_006719831.1:p.Ser338=
|
|
XM_011534938.2:c.924C>G
|
XP_011533240.1:p.Ser308=
|
|
XM_017020395.1:c.924C>G
|
XP_016875884.1:p.Ser308=
|
|
NM_194318.4:c.1071C>G
MANE Select
|
NP_919299.3:p.Ser357=
|
|