ENST00000309755.9:c.1114G>C
MANE Select
|
ENSP00000312397.4:p.Asp372His
|
|
ENST00000309755.8:c.1114G>C
|
ENSP00000312397.4:p.Asp372His
|
|
ENST00000502381.1:n.701G>C
|
|
|
ENST00000504208.5:c.*335-10621G>C
|
ENSP00000423585.1:n.*335-10621G>C
|
|
ENST00000505853.1:c.994G>C
|
ENSP00000426173.1:p.Asp332His
|
|
ENST00000506491.5:c.868G>C
|
ENSP00000424828.1:p.Asp290His
|
|
ENST00000506873.5:n.739G>C
|
|
|
ENST00000508657.5:c.1018G>C
|
ENSP00000422099.1:p.Asp340His
|
|
NM_001257194.1:c.1018G>C
|
NP_001244123.1:p.Asp340His
|
|
NM_001257195.1:c.868G>C
|
NP_001244124.1:p.Asp290His
|
|
NM_017415.2:c.1114G>C
|
NP_059111.2:p.Asp372His
|
|
NM_017415.3:c.1114G>C
MANE Select
|
NP_059111.2:p.Asp372His
|
|
NM_001257195.2:c.868G>C
|
NP_001244124.1:p.Asp290His
|
|