ENST00000682422.1:n.863C>G
|
|
|
ENST00000682545.1:c.*288C>G
|
ENSP00000508402.1:n.*288C>G
|
|
ENST00000682887.1:c.1683C>G
|
ENSP00000506946.1:n.1683C>G
|
|
ENST00000683302.1:c.1213C>G
|
ENSP00000507885.1:p.Leu405Val
|
|
ENST00000683557.1:c.*114C>G
|
ENSP00000508029.1:n.*114C>G
|
|
ENST00000367282.6:c.1282C>G
MANE Select
|
ENSP00000356251.4:p.Leu428Val
|
|
ENST00000367282.5:c.1282C>G
|
ENSP00000356251.4:p.Leu428Val
|
|
NM_004767.3:c.1282C>G
|
NP_004758.3:p.Leu428Val
|
|
XM_011510158.1:c.721C>G
|
XP_011508460.1:p.Leu241Val
|
|
NM_004767.4:c.1282C>G
|
NP_004758.3:p.Leu428Val
|
|
XM_011510158.2:c.721C>G
|
XP_011508460.1:p.Leu241Val
|
|
NM_004767.5:c.1282C>G
MANE Select
|
NP_004758.3:p.Leu428Val
|
|