NM_000791.4:c.392A>G
MANE Select
|
NP_000782.1:p.His131Arg
|
ENST00000439211.7:c.392A>G
MANE Select
|
ENSP00000396308.2:p.His131Arg
|
NM_000791.3:c.392A>G
|
NP_000782.1:p.His131Arg
|
NM_001290354.1:c.236A>G
|
NP_001277283.1:p.His79Arg
|
NM_001290354.2:c.236A>G
|
NP_001277283.1:p.His79Arg
|
NM_001290357.1:c.369+3913A>G
|
NP_001277286.1:n.369+3913A>G
|
NM_001290357.2:c.369+3913A>G
|
NP_001277286.1:n.369+3913A>G
|
NR_110936.1:n.707A>G
|
|
NR_110936.2:n.709A>G
|
|
ENST00000439211.6:c.392A>G
|
ENSP00000396308.2:p.His131Arg
|
ENST00000504396.1:c.236A>G
|
ENSP00000421334.1:p.His79Arg
|
ENST00000505337.5:c.392A>G
|
ENSP00000426474.1:p.His131Arg
|
ENST00000508282.1:n.350A>G
|
|
ENST00000511032.5:c.369+3913A>G
|
ENSP00000422732.1:n.369+3913A>G
|
ENST00000513048.5:n.273A>G
|
|