ENST00000644991.3:c.663G>C
MANE Select
|
ENSP00000495607.1:p.Glu221Asp
|
|
ENST00000614701.4:c.663G>C
|
ENSP00000482885.1:p.Glu221Asp
|
|
ENST00000616559.4:c.789G>C
|
ENSP00000483259.1:p.Glu263Asp
|
|
NM_001145026.1:c.663G>C
|
NP_001138498.1:p.Glu221Asp
|
|
XM_011538290.1:c.663G>C
|
XP_011536592.1:p.Glu221Asp
|
|
XM_017019273.1:c.1329G>C
|
XP_016874762.1:p.Glu443Asp
|
|
XM_017019274.1:c.1329G>C
|
XP_016874763.1:p.Glu443Asp
|
|
XM_017019275.1:c.1329G>C
|
XP_016874764.1:p.Glu443Asp
|
|
XR_001748688.1:n.1466G>C
|
|
|
XR_001748689.1:n.1466G>C
|
|
|
NM_001145026.2:c.663G>C
MANE Select
|
NP_001138498.1:p.Glu221Asp
|
|