ENST00000284885.8:c.2532T>A
MANE Select
|
ENSP00000284885.3:p.His844Gln
|
|
ENST00000284885.7:c.2532T>A
|
ENSP00000284885.3:p.His844Gln
|
|
NM_002772.2:c.2532T>A
|
NP_002763.2:p.His844Gln
|
|
XM_011529654.1:c.2667T>A
|
XP_011527956.1:p.His889Gln
|
|
XM_011529655.1:c.2667T>A
|
XP_011527957.1:p.His889Gln
|
|
XM_011529656.1:c.2667T>A
|
XP_011527958.1:p.His889Gln
|
|
XM_011529657.1:c.2622T>A
|
XP_011527959.1:p.His874Gln
|
|
XM_011529658.1:c.2586T>A
|
XP_011527960.1:p.His862Gln
|
|
XM_011529659.1:c.2577T>A
|
XP_011527961.1:p.His859Gln
|
|
XM_011529654.2:c.2667T>A
|
XP_011527956.1:p.His889Gln
|
|
XM_011529656.2:c.2667T>A
|
XP_011527958.1:p.His889Gln
|
|
XM_011529657.2:c.2622T>A
|
XP_011527959.1:p.His874Gln
|
|
XM_011529658.2:c.2586T>A
|
XP_011527960.1:p.His862Gln
|
|
NM_002772.3:c.2532T>A
MANE Select
|
NP_002763.3:p.His844Gln
|
|