ENST00000309755.9:c.1531G>C
MANE Select
|
ENSP00000312397.4:p.Asp511His
|
|
ENST00000309755.8:c.1531G>C
|
ENSP00000312397.4:p.Asp511His
|
|
ENST00000447439.6:n.1587G>C
|
|
|
ENST00000504208.5:c.*415G>C
|
ENSP00000423585.1:n.*415G>C
|
|
ENST00000506491.5:c.1285G>C
|
ENSP00000424828.1:p.Asp429His
|
|
ENST00000506873.5:n.1054G>C
|
|
|
ENST00000508657.5:c.1435G>C
|
ENSP00000422099.1:p.Asp479His
|
|
ENST00000509694.1:n.324G>C
|
|
|
NM_001257194.1:c.1435G>C
|
NP_001244123.1:p.Asp479His
|
|
NM_001257195.1:c.1285G>C
|
NP_001244124.1:p.Asp429His
|
|
NM_017415.2:c.1531G>C
|
NP_059111.2:p.Asp511His
|
|
NM_017415.3:c.1531G>C
MANE Select
|
NP_059111.2:p.Asp511His
|
|
NM_001257195.2:c.1285G>C
|
NP_001244124.1:p.Asp429His
|
|