ENST00000682422.1:n.898C>T
|
|
|
ENST00000682545.1:c.*323C>T
|
ENSP00000508402.1:n.*323C>T
|
|
ENST00000682887.1:c.1718C>T
|
ENSP00000506946.1:n.1718C>T
|
|
ENST00000683302.1:c.1248C>T
|
ENSP00000507885.1:p.Cys416=
|
|
ENST00000683557.1:c.*149C>T
|
ENSP00000508029.1:n.*149C>T
|
|
ENST00000367282.6:c.1317C>T
MANE Select
|
ENSP00000356251.4:p.Cys439=
|
|
ENST00000367282.5:c.1317C>T
|
ENSP00000356251.4:p.Cys439=
|
|
NM_004767.3:c.1317C>T
|
NP_004758.3:p.Cys439=
|
|
XM_011510158.1:c.756C>T
|
XP_011508460.1:p.Cys252=
|
|
NM_004767.4:c.1317C>T
|
NP_004758.3:p.Cys439=
|
|
XM_011510158.2:c.756C>T
|
XP_011508460.1:p.Cys252=
|
|
NM_004767.5:c.1317C>T
MANE Select
|
NP_004758.3:p.Cys439=
|
|