ENST00000258385.8:c.1360A=
MANE Select
|
ENSP00000258385.3:p.Asn454=
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|
ENST00000258385.7:c.1360A=
|
ENSP00000258385.3:p.Asn454=
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|
ENST00000441621.6:c.*542A=
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ENSP00000408819.2:n.*542A=
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|
ENST00000446616.1:c.*1001A=
|
ENSP00000410801.1:n.*1001A=
|
|
ENST00000543200.5:c.1315A=
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ENSP00000438380.1:p.Asn439=
|
|
NM_000751.2:c.1360A=
|
NP_000742.1:p.Asn454=
|
|
NM_001256657.1:c.1315A=
|
NP_001243586.1:p.Asn439=
|
|
NM_001311195.1:c.778A=
|
NP_001298124.1:p.Asn260=
|
|
NM_001311196.1:c.1057A=
|
NP_001298125.1:p.Asn353=
|
|
NR_046333.1:c.-4294966191A=
|
|
|
NR_046334.1:c.-4294965912A=
|
|
|
XM_011510524.1:c.979A=
|
XP_011508826.1:p.Asn327=
|
|
XM_011510524.2:c.979A=
|
XP_011508826.1:p.Asn327=
|
|
NM_000751.3:c.1360A=
MANE Select
|
NP_000742.1:p.Asn454=
|
|
NM_001311195.2:c.778A=
|
NP_001298124.1:p.Asn260=
|
|
NM_001311196.2:c.1057A=
|
NP_001298125.1:p.Asn353=
|
|
NM_001256657.2:c.1315A=
|
NP_001243586.1:p.Asn439=
|
|