ENST00000295897.9:c.1597T>G
MANE Select
|
ENSP00000295897.4:p.Phe533Val
|
|
ENST00000295897.8:c.1597T>G
|
ENSP00000295897.4:p.Phe533Val
|
|
ENST00000401494.7:c.1252T>G
|
ENSP00000384695.3:p.Phe418Val
|
|
ENST00000415165.6:c.1021T>G
|
ENSP00000401820.2:p.Phe341Val
|
|
ENST00000476441.6:c.*876T>G
|
ENSP00000423727.1:n.*876T>G
|
|
ENST00000486939.1:n.251T>G
|
|
|
ENST00000503124.5:c.1147T>G
|
ENSP00000421027.1:p.Phe383Val
|
|
ENST00000505649.5:n.1144T>G
|
|
|
ENST00000509063.5:c.1597T>G
|
ENSP00000422784.1:p.Phe533Val
|
|
ENST00000511370.1:c.1130T>G
|
|
|
ENST00000621085.4:c.958T>G
|
ENSP00000483421.1:p.Phe320Val
|
|
ENST00000621628.4:c.958T>G
|
ENSP00000480485.1:p.Phe320Val
|
|
NM_000477.5:c.1597T>G
|
NP_000468.1:p.Phe533Val
|
|
NM_000477.6:c.1597T>G
|
NP_000468.1:p.Phe533Val
|
|
NM_000477.7:c.1597T>G
MANE Select
|
NP_000468.1:p.Phe533Val
|
|