|
NM_004380.3:c.3955C>T
MANE Select
|
NP_004371.2:p.Arg1319Ter
|
|
ENST00000262367.10:c.3955C>T
MANE Select
|
ENSP00000262367.5:p.Arg1319Ter
|
|
NM_001079846.1:c.3841C>T
|
NP_001073315.1:p.Arg1281Ter
|
|
NM_004380.2:c.3955C>T
|
NP_004371.2:p.Arg1319Ter
|
|
ENST00000262367.9:c.3955C>T
|
ENSP00000262367.5:p.Arg1319Ter
|
|
ENST00000382070.7:c.3841C>T
|
ENSP00000371502.3:p.Arg1281Ter
|
|
ENST00000570939.2:c.2590C>T
|
ENSP00000461002.2:p.Arg864Ter
|
|
ENST00000572569.1:n.419C>T
|
|
|
ENST00000573517.6:c.261C>T
|
|
|
ENST00000574740.1:n.37C>T
|
|
|
ENST00000635919.1:n.3C>T
|
|
|
XM_005255124.3:c.3910C>T
|
XP_005255181.1:p.Arg1304Ter
|
|
XM_005255124.4:c.3910C>T
|
XP_005255181.1:p.Arg1304Ter
|
|
XM_005255125.3:c.3538C>T
|
XP_005255182.1:p.Arg1180Ter
|
|
XM_005255125.4:c.3538C>T
|
XP_005255182.1:p.Arg1180Ter
|
|
XM_006720848.2:c.3955C>T
|
XP_006720911.1:p.Arg1319Ter
|
|
XM_006720848.3:c.3955C>T
|
XP_006720911.1:p.Arg1319Ter
|
|
XM_011522380.1:c.3901C>T
|
XP_011520682.1:p.Arg1301Ter
|
|
XM_011522381.1:c.3202C>T
|
XP_011520683.1:p.Arg1068Ter
|
|
XM_011522381.2:c.3202C>T
|
XP_011520683.1:p.Arg1068Ter
|
|
XM_017022944.1:c.3949C>T
|
XP_016878433.1:p.Arg1317Ter
|