ENST00000262367.10:c.7250G>A
MANE Select
|
ENSP00000262367.5:p.Arg2417Lys
|
|
ENST00000262367.9:c.7250G>A
|
ENSP00000262367.5:p.Arg2417Lys
|
|
ENST00000382070.7:c.7136G>A
|
ENSP00000371502.3:p.Arg2379Lys
|
|
NM_001079846.1:c.7136G>A
|
NP_001073315.1:p.Arg2379Lys
|
|
NM_004380.2:c.7250G>A
|
NP_004371.2:p.Arg2417Lys
|
|
XM_005255124.3:c.7205G>A
|
XP_005255181.1:p.Arg2402Lys
|
|
XM_005255125.3:c.6833G>A
|
XP_005255182.1:p.Arg2278Lys
|
|
XM_006720848.2:c.6989G>A
|
XP_006720911.1:p.Arg2330Lys
|
|
XM_011522380.1:c.7196G>A
|
XP_011520682.1:p.Arg2399Lys
|
|
XM_011522381.1:c.6497G>A
|
XP_011520683.1:p.Arg2166Lys
|
|
XM_005255124.4:c.7205G>A
|
XP_005255181.1:p.Arg2402Lys
|
|
XM_005255125.4:c.6833G>A
|
XP_005255182.1:p.Arg2278Lys
|
|
XM_006720848.3:c.6989G>A
|
XP_006720911.1:p.Arg2330Lys
|
|
XM_011522381.2:c.6497G>A
|
XP_011520683.1:p.Arg2166Lys
|
|
XM_017022944.1:c.7244G>A
|
XP_016878433.1:p.Arg2415Lys
|
|
NM_004380.3:c.7250G>A
MANE Select
|
NP_004371.2:p.Arg2417Lys
|
|