ENST00000336906.6:c.238G>A
MANE Select
|
ENSP00000338082.4:p.Asp80Asn
|
|
ENST00000380252.6:c.73G>A
|
ENSP00000369602.2:p.Asp25Asn
|
|
ENST00000642908.1:c.238G>A
|
ENSP00000495346.1:p.Asp80Asn
|
|
ENST00000647543.1:c.238G>A
|
ENSP00000496470.1:p.Asp80Asn
|
|
ENST00000336906.4:c.238G>A
|
ENSP00000338082.4:p.Asp80Asn
|
|
ENST00000380252.5:c.208G>A
|
ENSP00000369602.1:p.Asp70Asn
|
|
ENST00000380259.6:c.238G>A
|
ENSP00000369609.2:p.Asp80Asn
|
|
ENST00000444587.1:c.*107G>A
|
ENSP00000488218.1:n.*107G>A
|
|
ENST00000620888.4:c.238G>A
|
ENSP00000479637.1:p.Asp80Asn
|
|
ENST00000624109.1:c.117C>T
|
ENSP00000485458.1:p.Ile39=
|
|
NM_000184.2:c.238G>A
|
NP_000175.1:p.Asp80Asn
|
|
NM_000184.3:c.238G>A
MANE Select
|
NP_000175.1:p.Asp80Asn
|
|