ENST00000262367.10:c.2507T>G
MANE Select
|
ENSP00000262367.5:p.Leu836Arg
|
|
ENST00000262367.9:c.2507T>G
|
ENSP00000262367.5:p.Leu836Arg
|
|
ENST00000382070.7:c.2393T>G
|
ENSP00000371502.3:p.Leu798Arg
|
|
ENST00000570939.2:c.1112T>G
|
ENSP00000461002.2:p.Leu371Arg
|
|
NM_001079846.1:c.2393T>G
|
NP_001073315.1:p.Leu798Arg
|
|
NM_004380.2:c.2507T>G
|
NP_004371.2:p.Leu836Arg
|
|
XM_005255124.3:c.2462T>G
|
XP_005255181.1:p.Leu821Arg
|
|
XM_005255125.3:c.2464-1590T>G
|
XP_005255182.1:n.2464-1590T>G
|
|
XM_006720848.2:c.2507T>G
|
XP_006720911.1:p.Leu836Arg
|
|
XM_011522380.1:c.2453T>G
|
XP_011520682.1:p.Leu818Arg
|
|
XM_011522381.1:c.1754T>G
|
XP_011520683.1:p.Leu585Arg
|
|
XM_011522382.1:c.2507T>G
|
XP_011520684.1:p.Leu836Arg
|
|
XM_005255124.4:c.2462T>G
|
XP_005255181.1:p.Leu821Arg
|
|
XM_005255125.4:c.2464-1590T>G
|
XP_005255182.1:n.2464-1590T>G
|
|
XM_006720848.3:c.2507T>G
|
XP_006720911.1:p.Leu836Arg
|
|
XM_011522381.2:c.1754T>G
|
XP_011520683.1:p.Leu585Arg
|
|
XM_011522382.3:c.2507T>G
|
XP_011520684.1:p.Leu836Arg
|
|
XM_017022944.1:c.2501T>G
|
XP_016878433.1:p.Leu834Arg
|
|
NM_004380.3:c.2507T>G
MANE Select
|
NP_004371.2:p.Leu836Arg
|
|