ENST00000636937.2:c.1488G>T
|
ENSP00000516154.1:p.Lys496Asn
|
|
ENST00000268124.11:c.1488G>T
MANE Select
|
ENSP00000268124.5:p.Lys496Asn
|
|
ENST00000530292.3:c.1089G>T
|
ENSP00000432885.2:p.Lys363Asn
|
|
ENST00000635986.2:c.1488G>T
|
ENSP00000490653.2:p.Lys496Asn
|
|
ENST00000636774.1:c.*55G>T
|
ENSP00000489799.1:n.*55G>T
|
|
ENST00000637238.1:c.225G>T
|
ENSP00000490756.1:p.Lys75Asn
|
|
ENST00000637264.1:c.560G>T
|
|
|
ENST00000666746.1:c.1065G>T
|
|
|
ENST00000672071.1:n.1686G>T
|
|
|
ENST00000672923.2:n.1591G>T
|
|
|
ENST00000268124.9:c.1488G>T
|
ENSP00000268124.5:p.Lys496Asn
|
|
ENST00000442287.6:c.1488G>T
|
ENSP00000399851.2:p.Lys496Asn
|
|
ENST00000631044.2:c.*871G>T
|
ENSP00000486730.1:n.*871G>T
|
|
NM_001126131.1:c.1488G>T
|
NP_001119603.1:p.Lys496Asn
|
|
NM_002693.2:c.1488G>T
|
NP_002684.1:p.Lys496Asn
|
|
NM_001126131.2:c.1488G>T
|
NP_001119603.1:p.Lys496Asn
|
|
NM_002693.3:c.1488G>T
MANE Select
|
NP_002684.1:p.Lys496Asn
|
|