ENST00000309755.9:c.1494T>C
MANE Select
|
ENSP00000312397.4:p.His498=
|
|
ENST00000309755.8:c.1494T>C
|
ENSP00000312397.4:p.His498=
|
|
ENST00000447439.6:n.1550T>C
|
|
|
ENST00000504208.5:c.*378T>C
|
ENSP00000423585.1:n.*378T>C
|
|
ENST00000506491.5:c.1248T>C
|
ENSP00000424828.1:p.His416=
|
|
ENST00000506873.5:n.1017T>C
|
|
|
ENST00000508657.5:c.1398T>C
|
ENSP00000422099.1:p.His466=
|
|
ENST00000509694.1:n.287T>C
|
|
|
NM_001257194.1:c.1398T>C
|
NP_001244123.1:p.His466=
|
|
NM_001257195.1:c.1248T>C
|
NP_001244124.1:p.His416=
|
|
NM_017415.2:c.1494T>C
|
NP_059111.2:p.His498=
|
|
NM_017415.3:c.1494T>C
MANE Select
|
NP_059111.2:p.His498=
|
|
NM_001257195.2:c.1248T>C
|
NP_001244124.1:p.His416=
|
|