ENST00000262367.10:c.6952C>A
MANE Select
|
ENSP00000262367.5:p.Gln2318Lys
|
|
ENST00000262367.9:c.6952C>A
|
ENSP00000262367.5:p.Gln2318Lys
|
|
ENST00000382070.7:c.6838C>A
|
ENSP00000371502.3:p.Gln2280Lys
|
|
NM_001079846.1:c.6838C>A
|
NP_001073315.1:p.Gln2280Lys
|
|
NM_004380.2:c.6952C>A
|
NP_004371.2:p.Gln2318Lys
|
|
XM_005255124.3:c.6907C>A
|
XP_005255181.1:p.Gln2303Lys
|
|
XM_005255125.3:c.6535C>A
|
XP_005255182.1:p.Gln2179Lys
|
|
XM_006720848.2:c.6691C>A
|
XP_006720911.1:p.Gln2231Lys
|
|
XM_011522380.1:c.6898C>A
|
XP_011520682.1:p.Gln2300Lys
|
|
XM_011522381.1:c.6199C>A
|
XP_011520683.1:p.Gln2067Lys
|
|
XM_005255124.4:c.6907C>A
|
XP_005255181.1:p.Gln2303Lys
|
|
XM_005255125.4:c.6535C>A
|
XP_005255182.1:p.Gln2179Lys
|
|
XM_006720848.3:c.6691C>A
|
XP_006720911.1:p.Gln2231Lys
|
|
XM_011522381.2:c.6199C>A
|
XP_011520683.1:p.Gln2067Lys
|
|
XM_017022944.1:c.6946C>A
|
XP_016878433.1:p.Gln2316Lys
|
|
NM_004380.3:c.6952C>A
MANE Select
|
NP_004371.2:p.Gln2318Lys
|
|