|
NM_021239.3:c.1216G>C
MANE Select
|
NP_067062.1:p.Glu406Gln
|
|
ENST00000261973.12:c.1216G>C
MANE Select
|
ENSP00000261973.7:p.Glu406Gln
|
|
NM_021239.2:c.1216G>C
|
NP_067062.1:p.Glu406Gln
|
|
ENST00000261973.11:c.1216G>C
|
ENSP00000261973.7:p.Glu406Gln
|
|
ENST00000527432.5:c.1216G>C
|
ENSP00000431150.1:p.Glu406Gln
|
|
ENST00000528081.5:c.*768G>C
|
ENSP00000434444.1:n.*768G>C
|
|
ENST00000532683.5:n.4836G>C
|
|
|
XM_011537044.1:c.1216G>C
|
XP_011535346.1:p.Glu406Gln
|
|
XM_011537044.3:c.1216G>C
|
XP_011535346.1:p.Glu406Gln
|
|
XM_011537045.1:c.601G>C
|
XP_011535347.1:p.Glu201Gln
|
|
XM_024449680.1:c.601G>C
|
XP_024305448.1:p.Glu201Gln
|
|
XR_943501.1:n.1501G>C
|
|
|
XR_943501.3:n.1405G>C
|
|