ENST00000700061.1:c.4371T>G
|
|
|
ENST00000700062.1:c.4426+13602T>G
|
|
|
ENST00000700063.1:c.896T>G
|
|
|
ENST00000700064.1:c.2241T>G
|
|
|
ENST00000281513.10:c.6385T>G
MANE Select
|
ENSP00000281513.5:p.Phe2129Val
|
|
ENST00000281513.9:c.6385T>G
|
ENSP00000281513.5:p.Phe2129Val
|
|
ENST00000417461.5:c.512+13602T>G
|
ENSP00000392421.1:n.512+13602T>G
|
|
ENST00000442506.5:c.3528T>G
|
|
|
NM_015909.3:c.6385T>G
|
NP_056993.2:p.Phe2129Val
|
|
NR_052013.2:n.6280+13602T>G
|
|
|
XM_011510357.1:c.6256T>G
|
XP_011508659.1:p.Phe2086Val
|
|
XM_011510358.1:c.6385T>G
|
XP_011508660.1:p.Phe2129Val
|
|
XM_011510359.1:c.5746T>G
|
XP_011508661.1:p.Phe1916Val
|
|
XM_011510360.1:c.4186T>G
|
XP_011508662.1:p.Phe1396Val
|
|
XM_011510361.1:c.4177T>G
|
XP_011508663.1:p.Phe1393Val
|
|
XM_011510357.2:c.6256T>G
|
XP_011508659.1:p.Phe2086Val
|
|
XM_011510358.2:c.6385T>G
|
XP_011508660.1:p.Phe2129Val
|
|
XM_011510360.2:c.4186T>G
|
XP_011508662.1:p.Phe1396Val
|
|
XM_011510361.2:c.4177T>G
|
XP_011508663.1:p.Phe1393Val
|
|
XM_017004317.1:c.6385T>G
|
XP_016859806.1:p.Phe2129Val
|
|
XM_024452961.1:c.5746T>G
|
XP_024308729.1:p.Phe1916Val
|
|
NM_015909.4:c.6385T>G
MANE Select
|
NP_056993.2:p.Phe2129Val
|
|
NR_052013.3:n.6266+13602T>G
|
|
|