ENST00000356392.9:c.1334A>G
MANE Select
|
ENSP00000348757.3:p.His445Arg
|
|
ENST00000356392.8:c.1334A>G
|
ENSP00000348757.3:p.His445Arg
|
|
ENST00000586836.5:c.761A>G
|
ENSP00000467429.1:p.His254Arg
|
|
ENST00000591179.5:c.1154A>G
|
ENSP00000466800.1:p.His385Arg
|
|
ENST00000591345.5:c.*1253A>G
|
ENSP00000467313.1:n.*1253A>G
|
|
NM_001302453.1:c.1172A>G
|
NP_001289382.1:p.His391Arg
|
|
NM_001302454.1:c.1154A>G
|
NP_001289383.1:p.His385Arg
|
|
NM_145045.4:c.1334A>G
|
NP_659482.3:p.His445Arg
|
|
NM_145045.5:c.1334A>G
MANE Select
|
NP_659482.3:p.His445Arg
|
|
NM_001302454.2:c.1154A>G
|
NP_001289383.1:p.His385Arg
|
|