ENST00000682422.1:n.888G>A
|
|
|
ENST00000682545.1:c.*313G>A
|
ENSP00000508402.1:n.*313G>A
|
|
ENST00000682887.1:c.1708G>A
|
ENSP00000506946.1:n.1708G>A
|
|
ENST00000683302.1:c.1238G>A
|
ENSP00000507885.1:p.Cys413Tyr
|
|
ENST00000683557.1:c.*139G>A
|
ENSP00000508029.1:n.*139G>A
|
|
ENST00000367282.6:c.1307G>A
MANE Select
|
ENSP00000356251.4:p.Cys436Tyr
|
|
ENST00000367282.5:c.1307G>A
|
ENSP00000356251.4:p.Cys436Tyr
|
|
NM_004767.3:c.1307G>A
|
NP_004758.3:p.Cys436Tyr
|
|
XM_011510158.1:c.746G>A
|
XP_011508460.1:p.Cys249Tyr
|
|
NM_004767.4:c.1307G>A
|
NP_004758.3:p.Cys436Tyr
|
|
XM_011510158.2:c.746G>A
|
XP_011508460.1:p.Cys249Tyr
|
|
NM_004767.5:c.1307G>A
MANE Select
|
NP_004758.3:p.Cys436Tyr
|
|