ENST00000258385.8:c.1131G>A
MANE Select
|
ENSP00000258385.3:p.Arg377=
|
|
ENST00000258385.7:c.1131G>A
|
ENSP00000258385.3:p.Arg377=
|
|
ENST00000441621.6:c.*313G>A
|
ENSP00000408819.2:n.*313G>A
|
|
ENST00000446616.1:c.*772G>A
|
ENSP00000410801.1:n.*772G>A
|
|
ENST00000543200.5:c.1086G>A
|
ENSP00000438380.1:p.Arg362=
|
|
NM_000751.2:c.1131G>A
|
NP_000742.1:p.Arg377=
|
|
NM_001256657.1:c.1086G>A
|
NP_001243586.1:p.Arg362=
|
|
NM_001311195.1:c.549G>A
|
NP_001298124.1:p.Arg183=
|
|
NM_001311196.1:c.828G>A
|
NP_001298125.1:p.Arg276=
|
|
NR_046333.1:c.-4294966420G>A
|
|
|
NR_046334.1:c.-4294966141G>A
|
|
|
XM_011510524.1:c.750G>A
|
XP_011508826.1:p.Arg250=
|
|
XM_011510524.2:c.750G>A
|
XP_011508826.1:p.Arg250=
|
|
NM_000751.3:c.1131G>A
MANE Select
|
NP_000742.1:p.Arg377=
|
|
NM_001311195.2:c.549G>A
|
NP_001298124.1:p.Arg183=
|
|
NM_001311196.2:c.828G>A
|
NP_001298125.1:p.Arg276=
|
|
NM_001256657.2:c.1086G>A
|
NP_001243586.1:p.Arg362=
|
|