ENST00000258385.8:c.1140C>T
MANE Select
|
ENSP00000258385.3:p.Ser380=
|
|
ENST00000258385.7:c.1140C>T
|
ENSP00000258385.3:p.Ser380=
|
|
ENST00000441621.6:c.*322C>T
|
ENSP00000408819.2:n.*322C>T
|
|
ENST00000446616.1:c.*781C>T
|
ENSP00000410801.1:n.*781C>T
|
|
ENST00000543200.5:c.1095C>T
|
ENSP00000438380.1:p.Ser365=
|
|
NM_000751.2:c.1140C>T
|
NP_000742.1:p.Ser380=
|
|
NM_001256657.1:c.1095C>T
|
NP_001243586.1:p.Ser365=
|
|
NM_001311195.1:c.558C>T
|
NP_001298124.1:p.Ser186=
|
|
NM_001311196.1:c.837C>T
|
NP_001298125.1:p.Ser279=
|
|
NR_046333.1:c.-4294966411C>T
|
|
|
NR_046334.1:c.-4294966132C>T
|
|
|
XM_011510524.1:c.759C>T
|
XP_011508826.1:p.Ser253=
|
|
XM_011510524.2:c.759C>T
|
XP_011508826.1:p.Ser253=
|
|
NM_000751.3:c.1140C>T
MANE Select
|
NP_000742.1:p.Ser380=
|
|
NM_001311195.2:c.558C>T
|
NP_001298124.1:p.Ser186=
|
|
NM_001311196.2:c.837C>T
|
NP_001298125.1:p.Ser279=
|
|
NM_001256657.2:c.1095C>T
|
NP_001243586.1:p.Ser365=
|
|