ENST00000312251.8:c.895T>G
MANE Select
|
ENSP00000310998.3:p.Leu299Val
|
|
ENST00000649828.1:c.895T>G
|
ENSP00000498032.1:p.Leu299Val
|
|
ENST00000312251.7:c.895T>G
|
ENSP00000310998.3:p.Leu299Val
|
|
ENST00000381955.7:c.895T>G
|
ENSP00000371381.3:p.Leu299Val
|
|
ENST00000562346.2:c.505-720T>G
|
|
|
ENST00000562746.5:c.895T>G
|
ENSP00000455900.1:p.Leu299Val
|
|
ENST00000563578.5:c.713T>G
|
|
|
ENST00000564397.5:n.1254T>G
|
|
|
ENST00000565876.5:c.480+1480T>G
|
|
|
ENST00000567739.5:n.214T>G
|
|
|
ENST00000568202.5:n.758T>G
|
|
|
ENST00000569296.5:c.439T>G
|
ENSP00000465949.1:p.Leu147Val
|
|
NM_016256.3:c.895T>G
|
NP_057340.2:p.Leu299Val
|
|
XM_011522517.1:c.895T>G
|
XP_011520819.1:p.Leu299Val
|
|
XM_011522518.1:c.895T>G
|
XP_011520820.1:p.Leu299Val
|
|
XM_011522519.1:c.895T>G
|
XP_011520821.1:p.Leu299Val
|
|
XR_243285.1:n.922T>G
|
|
|
XM_011522517.3:c.895T>G
|
XP_011520819.1:p.Leu299Val
|
|
XR_001751908.2:n.921T>G
|
|
|
XR_001751909.2:n.921T>G
|
|
|
XR_001751910.2:n.921T>G
|
|
|
XR_001751911.2:n.921T>G
|
|
|
XR_001751912.2:n.921T>G
|
|
|
NM_016256.4:c.895T>G
MANE Select
|
NP_057340.2:p.Leu299Val
|
|