ENST00000258385.8:c.1216G=
MANE Select
|
ENSP00000258385.3:p.Glu406=
|
|
ENST00000258385.7:c.1216G=
|
ENSP00000258385.3:p.Glu406=
|
|
ENST00000441621.6:c.*398G=
|
ENSP00000408819.2:n.*398G=
|
|
ENST00000446616.1:c.*857G=
|
ENSP00000410801.1:n.*857G=
|
|
ENST00000543200.5:c.1171G=
|
ENSP00000438380.1:p.Glu391=
|
|
NM_000751.2:c.1216G=
|
NP_000742.1:p.Glu406=
|
|
NM_001256657.1:c.1171G=
|
NP_001243586.1:p.Glu391=
|
|
NM_001311195.1:c.634G=
|
NP_001298124.1:p.Glu212=
|
|
NM_001311196.1:c.913G=
|
NP_001298125.1:p.Glu305=
|
|
NR_046333.1:c.-4294966335G=
|
|
|
NR_046334.1:c.-4294966056G=
|
|
|
XM_011510524.1:c.835G=
|
XP_011508826.1:p.Glu279=
|
|
XM_011510524.2:c.835G=
|
XP_011508826.1:p.Glu279=
|
|
NM_000751.3:c.1216G=
MANE Select
|
NP_000742.1:p.Glu406=
|
|
NM_001311195.2:c.634G=
|
NP_001298124.1:p.Glu212=
|
|
NM_001311196.2:c.913G=
|
NP_001298125.1:p.Glu305=
|
|
NM_001256657.2:c.1171G=
|
NP_001243586.1:p.Glu391=
|
|