ENST00000295897.9:c.1771T>A
MANE Select
|
ENSP00000295897.4:p.Cys591Ser
|
|
ENST00000295897.8:c.1771T>A
|
ENSP00000295897.4:p.Cys591Ser
|
|
ENST00000401494.7:c.1426T>A
|
ENSP00000384695.3:p.Cys476Ser
|
|
ENST00000415165.6:c.1195T>A
|
ENSP00000401820.2:p.Cys399Ser
|
|
ENST00000476441.6:c.*1050T>A
|
ENSP00000423727.1:n.*1050T>A
|
|
ENST00000495173.1:n.79T>A
|
|
|
ENST00000503124.5:c.1321T>A
|
ENSP00000421027.1:p.Cys441Ser
|
|
ENST00000505649.5:n.1318T>A
|
|
|
ENST00000508932.5:n.175+170T>A
|
|
|
ENST00000509063.5:c.1771T>A
|
ENSP00000422784.1:p.Cys591Ser
|
|
ENST00000511370.1:c.1304T>A
|
|
|
ENST00000621085.4:c.1132T>A
|
ENSP00000483421.1:p.Cys378Ser
|
|
ENST00000621628.4:c.1132T>A
|
ENSP00000480485.1:p.Cys378Ser
|
|
NM_000477.5:c.1771T>A
|
NP_000468.1:p.Cys591Ser
|
|
NM_000477.6:c.1771T>A
|
NP_000468.1:p.Cys591Ser
|
|
NM_000477.7:c.1771T>A
MANE Select
|
NP_000468.1:p.Cys591Ser
|
|