ENST00000258385.8:c.1234A>T
MANE Select
|
ENSP00000258385.3:p.Arg412Trp
|
|
ENST00000258385.7:c.1234A>T
|
ENSP00000258385.3:p.Arg412Trp
|
|
ENST00000441621.6:c.*416A>T
|
ENSP00000408819.2:n.*416A>T
|
|
ENST00000446616.1:c.*875A>T
|
ENSP00000410801.1:n.*875A>T
|
|
ENST00000543200.5:c.1189A>T
|
ENSP00000438380.1:p.Arg397Trp
|
|
NM_000751.2:c.1234A>T
|
NP_000742.1:p.Arg412Trp
|
|
NM_001256657.1:c.1189A>T
|
NP_001243586.1:p.Arg397Trp
|
|
NM_001311195.1:c.652A>T
|
NP_001298124.1:p.Arg218Trp
|
|
NM_001311196.1:c.931A>T
|
NP_001298125.1:p.Arg311Trp
|
|
NR_046333.1:c.-4294966317A>T
|
|
|
NR_046334.1:c.-4294966038A>T
|
|
|
XM_011510524.1:c.853A>T
|
XP_011508826.1:p.Arg285Trp
|
|
XM_011510524.2:c.853A>T
|
XP_011508826.1:p.Arg285Trp
|
|
NM_000751.3:c.1234A>T
MANE Select
|
NP_000742.1:p.Arg412Trp
|
|
NM_001311195.2:c.652A>T
|
NP_001298124.1:p.Arg218Trp
|
|
NM_001311196.2:c.931A>T
|
NP_001298125.1:p.Arg311Trp
|
|
NM_001256657.2:c.1189A>T
|
NP_001243586.1:p.Arg397Trp
|
|