ENST00000343307.5:c.1107C>T
MANE Select
|
ENSP00000343002.4:p.Gly369=
|
|
ENST00000343307.4:c.1107C>T
|
ENSP00000343002.4:p.Gly369=
|
|
NM_194318.3:c.1107C>T
|
NP_919299.3:p.Gly369=
|
|
XM_006719768.2:c.1050C>T
|
XP_006719831.1:p.Gly350=
|
|
XM_011534936.1:c.1065-6143C>T
|
XP_011533238.1:n.1065-6143C>T
|
|
XM_011534937.1:c.987C>T
|
XP_011533239.1:p.Gly329=
|
|
XM_011534938.1:c.960C>T
|
XP_011533240.1:p.Gly320=
|
|
XR_941500.1:n.1292C>T
|
|
|
XR_941501.1:n.1172C>T
|
|
|
XM_006719768.3:c.1050C>T
|
XP_006719831.1:p.Gly350=
|
|
XM_011534938.2:c.960C>T
|
XP_011533240.1:p.Gly320=
|
|
XM_017020395.1:c.960C>T
|
XP_016875884.1:p.Gly320=
|
|
NM_194318.4:c.1107C>T
MANE Select
|
NP_919299.3:p.Gly369=
|
|