ENST00000262367.10:c.7015C>G
MANE Select
|
ENSP00000262367.5:p.Leu2339Val
|
|
ENST00000262367.9:c.7015C>G
|
ENSP00000262367.5:p.Leu2339Val
|
|
ENST00000382070.7:c.6901C>G
|
ENSP00000371502.3:p.Leu2301Val
|
|
NM_001079846.1:c.6901C>G
|
NP_001073315.1:p.Leu2301Val
|
|
NM_004380.2:c.7015C>G
|
NP_004371.2:p.Leu2339Val
|
|
XM_005255124.3:c.6970C>G
|
XP_005255181.1:p.Leu2324Val
|
|
XM_005255125.3:c.6598C>G
|
XP_005255182.1:p.Leu2200Val
|
|
XM_006720848.2:c.6754C>G
|
XP_006720911.1:p.Leu2252Val
|
|
XM_011522380.1:c.6961C>G
|
XP_011520682.1:p.Leu2321Val
|
|
XM_011522381.1:c.6262C>G
|
XP_011520683.1:p.Leu2088Val
|
|
XM_005255124.4:c.6970C>G
|
XP_005255181.1:p.Leu2324Val
|
|
XM_005255125.4:c.6598C>G
|
XP_005255182.1:p.Leu2200Val
|
|
XM_006720848.3:c.6754C>G
|
XP_006720911.1:p.Leu2252Val
|
|
XM_011522381.2:c.6262C>G
|
XP_011520683.1:p.Leu2088Val
|
|
XM_017022944.1:c.7009C>G
|
XP_016878433.1:p.Leu2337Val
|
|
NM_004380.3:c.7015C>G
MANE Select
|
NP_004371.2:p.Leu2339Val
|
|