ENST00000078445.7:c.531T>C
MANE Select
|
ENSP00000078445.1:p.Asn177=
|
|
ENST00000078445.6:c.531T>C
|
ENSP00000078445.1:p.Asn177=
|
|
ENST00000595923.5:c.528T>C
|
ENSP00000469355.1:p.Asn176=
|
|
ENST00000602147.1:c.531T>C
|
ENSP00000470119.1:p.Asn177=
|
|
ENST00000602257.5:c.531T>C
|
ENSP00000472399.1:p.Asn177=
|
|
NM_001271995.1:c.528T>C
|
NP_001258924.1:p.Asn176=
|
|
NM_001271996.1:c.531T>C
|
NP_001258925.1:p.Asn177=
|
|
NM_001271997.1:c.531T>C
|
NP_001258926.1:p.Asn177=
|
|
NM_032607.2:c.531T>C
|
NP_115996.1:p.Asn177=
|
|
NM_032607.3:c.531T>C
MANE Select
|
NP_115996.1:p.Asn177=
|
|
NM_001271995.2:c.528T>C
|
NP_001258924.1:p.Asn176=
|
|
NM_001271996.2:c.531T>C
|
NP_001258925.1:p.Asn177=
|
|
NM_001271997.2:c.531T>C
|
NP_001258926.1:p.Asn177=
|
|