ENST00000294288.5:c.346G>C
MANE Select
|
ENSP00000294288.4:p.Glu116Gln
|
|
ENST00000545205.2:c.*131G>C
|
ENSP00000446180.1:n.*131G>C
|
|
ENST00000636477.1:c.298G>C
|
ENSP00000490746.1:p.Glu100Gln
|
|
ENST00000294288.4:c.346G>C
|
ENSP00000294288.4:p.Glu116Gln
|
|
ENST00000353903.9:c.175G>C
|
ENSP00000312037.4:p.Glu59Gln
|
|
ENST00000545205.1:c.*131G>C
|
ENSP00000446180.1:n.*131G>C
|
|
NM_016366.2:c.346G>C
|
NP_057450.2:p.Glu116Gln
|
|
XM_005274046.1:c.364G>C
|
XP_005274103.1:p.Glu122Gln
|
|
NM_001318496.1:c.364G>C
|
NP_001305425.1:p.Glu122Gln
|
|
NM_001318496.2:c.364G>C
|
NP_001305425.1:p.Glu122Gln
|
|
NM_016366.3:c.346G>C
MANE Select
|
NP_057450.2:p.Glu116Gln
|
|