ENST00000262367.10:c.3582G>T
MANE Select
|
ENSP00000262367.5:p.Gln1194His
|
|
ENST00000262367.9:c.3582G>T
|
ENSP00000262367.5:p.Gln1194His
|
|
ENST00000382070.7:c.3468G>T
|
ENSP00000371502.3:p.Gln1156His
|
|
ENST00000570939.2:c.2187G>T
|
ENSP00000461002.2:p.Gln729His
|
|
NM_001079846.1:c.3468G>T
|
NP_001073315.1:p.Gln1156His
|
|
NM_004380.2:c.3582G>T
|
NP_004371.2:p.Gln1194His
|
|
XM_005255124.3:c.3537G>T
|
XP_005255181.1:p.Gln1179His
|
|
XM_005255125.3:c.3165G>T
|
XP_005255182.1:p.Gln1055His
|
|
XM_006720848.2:c.3582G>T
|
XP_006720911.1:p.Gln1194His
|
|
XM_011522380.1:c.3528G>T
|
XP_011520682.1:p.Gln1176His
|
|
XM_011522381.1:c.2829G>T
|
XP_011520683.1:p.Gln943His
|
|
XM_011522382.1:c.3582G>T
|
XP_011520684.1:p.Gln1194His
|
|
XM_005255124.4:c.3537G>T
|
XP_005255181.1:p.Gln1179His
|
|
XM_005255125.4:c.3165G>T
|
XP_005255182.1:p.Gln1055His
|
|
XM_006720848.3:c.3582G>T
|
XP_006720911.1:p.Gln1194His
|
|
XM_011522381.2:c.2829G>T
|
XP_011520683.1:p.Gln943His
|
|
XM_011522382.3:c.3582G>T
|
XP_011520684.1:p.Gln1194His
|
|
XM_017022944.1:c.3576G>T
|
XP_016878433.1:p.Gln1192His
|
|
NM_004380.3:c.3582G>T
MANE Select
|
NP_004371.2:p.Gln1194His
|
|