ENST00000696133.1:c.1292A=
|
ENSP00000512426.1:p.Asn431=
|
|
ENST00000696134.1:c.*719A=
|
ENSP00000512427.1:n.*719A=
|
|
ENST00000367021.8:c.1292A=
MANE Select
|
ENSP00000355988.3:p.Asn431=
|
|
ENST00000643798.1:c.*802A=
|
ENSP00000496669.1:n.*802A=
|
|
ENST00000367021.7:c.1292A=
|
ENSP00000355988.3:p.Asn431=
|
|
ENST00000542854.5:c.1007A=
|
ENSP00000440532.1:p.Asn336=
|
|
NM_001206696.1:c.1007A=
|
NP_001193625.1:p.Asn336=
|
|
NM_006147.3:c.1292A=
|
NP_006138.1:p.Asn431=
|
|
NM_006147.4:c.1292A=
MANE Select
|
NP_006138.1:p.Asn431=
|
|
NM_001206696.2:c.1007A=
|
NP_001193625.1:p.Asn336=
|
|