ENST00000258385.8:c.1358A>C
MANE Select
|
ENSP00000258385.3:p.Asn453Thr
|
|
ENST00000258385.7:c.1358A>C
|
ENSP00000258385.3:p.Asn453Thr
|
|
ENST00000441621.6:c.*540A>C
|
ENSP00000408819.2:n.*540A>C
|
|
ENST00000446616.1:c.*999A>C
|
ENSP00000410801.1:n.*999A>C
|
|
ENST00000543200.5:c.1313A>C
|
ENSP00000438380.1:p.Asn438Thr
|
|
NM_000751.2:c.1358A>C
|
NP_000742.1:p.Asn453Thr
|
|
NM_001256657.1:c.1313A>C
|
NP_001243586.1:p.Asn438Thr
|
|
NM_001311195.1:c.776A>C
|
NP_001298124.1:p.Asn259Thr
|
|
NM_001311196.1:c.1055A>C
|
NP_001298125.1:p.Asn352Thr
|
|
NR_046333.1:c.-4294966193A>C
|
|
|
NR_046334.1:c.-4294965914A>C
|
|
|
XM_011510524.1:c.977A>C
|
XP_011508826.1:p.Asn326Thr
|
|
XM_011510524.2:c.977A>C
|
XP_011508826.1:p.Asn326Thr
|
|
NM_000751.3:c.1358A>C
MANE Select
|
NP_000742.1:p.Asn453Thr
|
|
NM_001311195.2:c.776A>C
|
NP_001298124.1:p.Asn259Thr
|
|
NM_001311196.2:c.1055A>C
|
NP_001298125.1:p.Asn352Thr
|
|
NM_001256657.2:c.1313A>C
|
NP_001243586.1:p.Asn438Thr
|
|