ENST00000682422.1:n.906C>T
|
|
|
ENST00000682545.1:c.*331C>T
|
ENSP00000508402.1:n.*331C>T
|
|
ENST00000682887.1:c.1726C>T
|
ENSP00000506946.1:n.1726C>T
|
|
ENST00000683302.1:c.1256C>T
|
ENSP00000507885.1:p.Ala419Val
|
|
ENST00000683557.1:c.*157C>T
|
ENSP00000508029.1:n.*157C>T
|
|
ENST00000367282.6:c.1325C>T
MANE Select
|
ENSP00000356251.4:p.Ala442Val
|
|
ENST00000367282.5:c.1325C>T
|
ENSP00000356251.4:p.Ala442Val
|
|
NM_004767.3:c.1325C>T
|
NP_004758.3:p.Ala442Val
|
|
XM_011510158.1:c.764C>T
|
XP_011508460.1:p.Ala255Val
|
|
NM_004767.4:c.1325C>T
|
NP_004758.3:p.Ala442Val
|
|
XM_011510158.2:c.764C>T
|
XP_011508460.1:p.Ala255Val
|
|
NM_004767.5:c.1325C>T
MANE Select
|
NP_004758.3:p.Ala442Val
|
|