ENST00000682422.1:n.770C>G
|
|
|
ENST00000682545.1:c.*195C>G
|
ENSP00000508402.1:n.*195C>G
|
|
ENST00000682887.1:c.1590C>G
|
ENSP00000506946.1:n.1590C>G
|
|
ENST00000683302.1:c.1120C>G
|
ENSP00000507885.1:p.Leu374Val
|
|
ENST00000683557.1:c.*21C>G
|
ENSP00000508029.1:n.*21C>G
|
|
ENST00000367282.6:c.1189C>G
MANE Select
|
ENSP00000356251.4:p.Leu397Val
|
|
ENST00000367282.5:c.1189C>G
|
ENSP00000356251.4:p.Leu397Val
|
|
NM_004767.3:c.1189C>G
|
NP_004758.3:p.Leu397Val
|
|
XM_011510158.1:c.628C>G
|
XP_011508460.1:p.Leu210Val
|
|
NM_004767.4:c.1189C>G
|
NP_004758.3:p.Leu397Val
|
|
XM_011510158.2:c.628C>G
|
XP_011508460.1:p.Leu210Val
|
|
NM_004767.5:c.1189C>G
MANE Select
|
NP_004758.3:p.Leu397Val
|
|