ENST00000217958.8:c.556G>C
MANE Select
|
ENSP00000217958.3:p.Glu186Gln
|
|
ENST00000217958.7:c.556G>C
|
ENSP00000217958.3:p.Glu186Gln
|
|
ENST00000340200.5:c.457G>C
|
ENSP00000345963.5:p.Glu153Gln
|
|
ENST00000361815.9:c.*21G>C
|
ENSP00000354906.5:n.*21G>C
|
|
ENST00000372295.5:c.433G>C
|
ENSP00000361369.1:p.Glu145Gln
|
|
ENST00000372296.5:c.*21G>C
|
ENSP00000361370.1:n.*21G>C
|
|
NM_002814.3:c.556G>C
|
NP_002805.1:p.Glu186Gln
|
|
NM_170750.2:c.*21G>C
|
NP_736606.1:n.*21G>C
|
|
NM_002814.4:c.556G>C
MANE Select
|
NP_002805.1:p.Glu186Gln
|
|
NM_170750.3:c.*21G>C
|
NP_736606.1:n.*21G>C
|
|