ENST00000355773.6:c.976G>C
MANE Select
|
ENSP00000348019.5:p.Glu326Gln
|
|
ENST00000355773.5:c.976G>C
|
ENSP00000348019.5:p.Glu326Gln
|
|
NM_012434.4:c.976G>C
|
NP_036566.1:p.Glu326Gln
|
|
XM_005248710.2:c.925G>C
|
XP_005248767.1:p.Glu309Gln
|
|
XM_005248711.1:c.778G>C
|
XP_005248768.1:p.Glu260Gln
|
|
XM_011535750.1:c.976G>C
|
XP_011534052.1:p.Glu326Gln
|
|
NM_012434.5:c.976G>C
MANE Select
|
NP_036566.1:p.Glu326Gln
|
|
NM_001382629.1:c.745G>C
|
NP_001369558.1:p.Glu249Gln
|
|
NM_001382630.1:c.976G>C
|
NP_001369559.1:p.Glu326Gln
|
|
NM_001382631.1:c.997G>C
|
NP_001369560.1:p.Glu333Gln
|
|
NM_001382632.1:c.889G>C
|
NP_001369561.1:p.Glu297Gln
|
|
NM_001382633.1:c.976G>C
|
NP_001369562.1:p.Glu326Gln
|
|
NM_001382634.1:c.820-6359G>C
|
NP_001369563.1:n.820-6359G>C
|
|
NM_001382635.1:c.973G>C
|
NP_001369564.1:p.Glu325Gln
|
|
NM_001382636.1:c.658G>C
|
NP_001369565.1:p.Glu220Gln
|
|