ENST00000682422.1:n.912A>C
|
|
|
ENST00000682545.1:c.*337A>C
|
ENSP00000508402.1:n.*337A>C
|
|
ENST00000682887.1:c.1732A>C
|
ENSP00000506946.1:n.1732A>C
|
|
ENST00000683302.1:c.1262A>C
|
ENSP00000507885.1:p.Glu421Ala
|
|
ENST00000683557.1:c.*163A>C
|
ENSP00000508029.1:n.*163A>C
|
|
ENST00000367282.6:c.1331A>C
MANE Select
|
ENSP00000356251.4:p.Glu444Ala
|
|
ENST00000367282.5:c.1331A>C
|
ENSP00000356251.4:p.Glu444Ala
|
|
NM_004767.3:c.1331A>C
|
NP_004758.3:p.Glu444Ala
|
|
XM_011510158.1:c.770A>C
|
XP_011508460.1:p.Glu257Ala
|
|
NM_004767.4:c.1331A>C
|
NP_004758.3:p.Glu444Ala
|
|
XM_011510158.2:c.770A>C
|
XP_011508460.1:p.Glu257Ala
|
|
NM_004767.5:c.1331A>C
MANE Select
|
NP_004758.3:p.Glu444Ala
|
|