ENST00000295897.9:c.1761T>G
MANE Select
|
ENSP00000295897.4:p.Asp587Glu
|
|
ENST00000295897.8:c.1761T>G
|
ENSP00000295897.4:p.Asp587Glu
|
|
ENST00000401494.7:c.1416T>G
|
ENSP00000384695.3:p.Asp472Glu
|
|
ENST00000415165.6:c.1185T>G
|
ENSP00000401820.2:p.Asp395Glu
|
|
ENST00000476441.6:c.*1040T>G
|
ENSP00000423727.1:n.*1040T>G
|
|
ENST00000495173.1:n.69T>G
|
|
|
ENST00000503124.5:c.1311T>G
|
ENSP00000421027.1:p.Asp437Glu
|
|
ENST00000505649.5:n.1308T>G
|
|
|
ENST00000508932.5:n.175+160T>G
|
|
|
ENST00000509063.5:c.1761T>G
|
ENSP00000422784.1:p.Asp587Glu
|
|
ENST00000511370.1:c.1294T>G
|
|
|
ENST00000621085.4:c.1122T>G
|
ENSP00000483421.1:p.Asp374Glu
|
|
ENST00000621628.4:c.1122T>G
|
ENSP00000480485.1:p.Asp374Glu
|
|
NM_000477.5:c.1761T>G
|
NP_000468.1:p.Asp587Glu
|
|
NM_000477.6:c.1761T>G
|
NP_000468.1:p.Asp587Glu
|
|
NM_000477.7:c.1761T>G
MANE Select
|
NP_000468.1:p.Asp587Glu
|
|