ENST00000265517.10:c.2612A>G
MANE Select
|
ENSP00000265517.5:p.His871Arg
|
|
ENST00000457717.6:c.2612A>G
|
ENSP00000400821.1:p.His871Arg
|
|
ENST00000511045.6:c.2363A>G
|
ENSP00000427679.2:p.His788Arg
|
|
ENST00000265517.9:c.2612A>G
|
ENSP00000265517.5:p.His871Arg
|
|
ENST00000457717.5:c.2612A>G
|
ENSP00000400821.1:p.His871Arg
|
|
ENST00000511045.5:c.2693A>G
|
ENSP00000427679.1:p.His898Arg
|
|
ENST00000619629.1:c.*1059A>G
|
ENSP00000482850.1:n.*1059A>G
|
|
NM_000253.3:c.2612A>G
|
NP_000244.2:p.His871Arg
|
|
NM_001300785.1:c.2693A>G
|
NP_001287714.1:p.His898Arg
|
|
NM_000253.4:c.2612A>G
|
NP_000244.2:p.His871Arg
|
|
NM_001300785.2:c.2363A>G
|
NP_001287714.2:p.His788Arg
|
|
NM_001386140.1:c.2612A>G
MANE Select
|
NP_001373069.1:p.His871Arg
|
|