ENST00000305046.13:c.169A>T
MANE Select
|
ENSP00000306606.8:p.Asn57Tyr
|
|
ENST00000639454.1:c.169A>T
|
ENSP00000491622.1:p.Asn57Tyr
|
|
ENST00000305046.12:c.169A>T
|
ENSP00000306606.8:p.Asn57Tyr
|
|
ENST00000504498.1:n.223A>T
|
|
|
ENST00000506651.5:c.49A>T
|
ENSP00000425998.2:p.Asn17Tyr
|
|
ENST00000515694.4:n.2264A>T
|
|
|
ENST00000625860.2:c.49A>T
|
ENSP00000486614.1:p.Asn17Tyr
|
|
ENST00000632775.1:n.732A>T
|
|
|
NM_000668.5:c.169A>T
|
NP_000659.2:p.Asn57Tyr
|
|
NM_001286650.1:c.49A>T
|
NP_001273579.1:p.Asn17Tyr
|
|
NM_000668.6:c.169A>T
MANE Select
|
NP_000659.2:p.Asn57Tyr
|
|
NM_001286650.2:c.49A>T
|
NP_001273579.1:p.Asn17Tyr
|
|