ENST00000309755.9:c.1113G>C
MANE Select
|
ENSP00000312397.4:p.Lys371Asn
|
|
ENST00000309755.8:c.1113G>C
|
ENSP00000312397.4:p.Lys371Asn
|
|
ENST00000502381.1:n.700G>C
|
|
|
ENST00000504208.5:c.*335-10622G>C
|
ENSP00000423585.1:n.*335-10622G>C
|
|
ENST00000505853.1:c.993G>C
|
ENSP00000426173.1:p.Lys331Asn
|
|
ENST00000506491.5:c.867G>C
|
ENSP00000424828.1:p.Lys289Asn
|
|
ENST00000506873.5:n.738G>C
|
|
|
ENST00000508657.5:c.1017G>C
|
ENSP00000422099.1:p.Lys339Asn
|
|
NM_001257194.1:c.1017G>C
|
NP_001244123.1:p.Lys339Asn
|
|
NM_001257195.1:c.867G>C
|
NP_001244124.1:p.Lys289Asn
|
|
NM_017415.2:c.1113G>C
|
NP_059111.2:p.Lys371Asn
|
|
NM_017415.3:c.1113G>C
MANE Select
|
NP_059111.2:p.Lys371Asn
|
|
NM_001257195.2:c.867G>C
|
NP_001244124.1:p.Lys289Asn
|
|