ENST00000259216.6:c.661C>A
MANE Select
|
ENSP00000259216.5:p.His221Asn
|
|
ENST00000259216.4:c.661C>A
|
ENSP00000259216.4:p.His221Asn
|
|
ENST00000615342.4:c.546C>A
|
ENSP00000480526.1:p.Gly182=
|
|
ENST00000621673.4:c.436C>A
|
ENSP00000480843.1:p.His146Asn
|
|
NM_001270420.1:c.546C>A
|
NP_001257349.1:p.Gly182=
|
|
NM_001270421.1:c.436C>A
|
NP_001257350.1:p.His146Asn
|
|
NM_032545.3:c.661C>A
|
NP_115934.1:p.His221Asn
|
|
NM_032545.4:c.661C>A
MANE Select
|
NP_115934.1:p.His221Asn
|
|
NM_001270420.2:c.546C>A
|
NP_001257349.1:p.Gly182=
|
|
NM_001270421.2:c.436C>A
|
NP_001257350.1:p.His146Asn
|
|