ENST00000262367.10:c.3613G>C
MANE Select
|
ENSP00000262367.5:p.Glu1205Gln
|
|
ENST00000262367.9:c.3613G>C
|
ENSP00000262367.5:p.Glu1205Gln
|
|
ENST00000382070.7:c.3499G>C
|
ENSP00000371502.3:p.Glu1167Gln
|
|
ENST00000570939.2:c.2218G>C
|
ENSP00000461002.2:p.Glu740Gln
|
|
NM_001079846.1:c.3499G>C
|
NP_001073315.1:p.Glu1167Gln
|
|
NM_004380.2:c.3613G>C
|
NP_004371.2:p.Glu1205Gln
|
|
XM_005255124.3:c.3568G>C
|
XP_005255181.1:p.Glu1190Gln
|
|
XM_005255125.3:c.3196G>C
|
XP_005255182.1:p.Glu1066Gln
|
|
XM_006720848.2:c.3613G>C
|
XP_006720911.1:p.Glu1205Gln
|
|
XM_011522380.1:c.3559G>C
|
XP_011520682.1:p.Glu1187Gln
|
|
XM_011522381.1:c.2860G>C
|
XP_011520683.1:p.Glu954Gln
|
|
XM_011522382.1:c.3613G>C
|
XP_011520684.1:p.Glu1205Gln
|
|
XM_005255124.4:c.3568G>C
|
XP_005255181.1:p.Glu1190Gln
|
|
XM_005255125.4:c.3196G>C
|
XP_005255182.1:p.Glu1066Gln
|
|
XM_006720848.3:c.3613G>C
|
XP_006720911.1:p.Glu1205Gln
|
|
XM_011522381.2:c.2860G>C
|
XP_011520683.1:p.Glu954Gln
|
|
XM_011522382.3:c.3613G>C
|
XP_011520684.1:p.Glu1205Gln
|
|
XM_017022944.1:c.3607G>C
|
XP_016878433.1:p.Glu1203Gln
|
|
NM_004380.3:c.3613G>C
MANE Select
|
NP_004371.2:p.Glu1205Gln
|
|