ENST00000636937.2:c.1585G>A
|
ENSP00000516154.1:p.Asp529Asn
|
|
ENST00000268124.11:c.1585G>A
MANE Select
|
ENSP00000268124.5:p.Asp529Asn
|
|
ENST00000530292.3:c.1186G>A
|
ENSP00000432885.2:p.Asp396Asn
|
|
ENST00000635986.2:c.1585G>A
|
ENSP00000490653.2:p.Asp529Asn
|
|
ENST00000636774.1:c.*152G>A
|
ENSP00000489799.1:n.*152G>A
|
|
ENST00000637238.1:c.322G>A
|
ENSP00000490756.1:p.Asp108Asn
|
|
ENST00000637264.1:c.657G>A
|
|
|
ENST00000666746.1:c.1162G>A
|
|
|
ENST00000672071.1:n.1783G>A
|
|
|
ENST00000672923.2:n.1688G>A
|
|
|
ENST00000268124.9:c.1585G>A
|
ENSP00000268124.5:p.Asp529Asn
|
|
ENST00000442287.6:c.1585G>A
|
ENSP00000399851.2:p.Asp529Asn
|
|
ENST00000631044.2:c.*968G>A
|
ENSP00000486730.1:n.*968G>A
|
|
NM_001126131.1:c.1585G>A
|
NP_001119603.1:p.Asp529Asn
|
|
NM_002693.2:c.1585G>A
|
NP_002684.1:p.Asp529Asn
|
|
NM_001126131.2:c.1585G>A
|
NP_001119603.1:p.Asp529Asn
|
|
NM_002693.3:c.1585G>A
MANE Select
|
NP_002684.1:p.Asp529Asn
|
|