ENST00000695651.1:n.2282C>G
|
|
|
ENST00000695653.1:c.1843C>G
|
ENSP00000512084.1:p.His615Asp
|
|
ENST00000695654.1:c.2959C>G
|
ENSP00000512085.1:p.His987Asp
|
|
ENST00000695690.1:n.125C>G
|
|
|
ENST00000695691.1:n.125C>G
|
|
|
ENST00000245907.11:c.3934C>G
MANE Select
|
ENSP00000245907.4:p.His1312Asp
|
|
ENST00000245907.10:c.3934C>G
|
ENSP00000245907.4:p.His1312Asp
|
|
ENST00000596238.1:n.377C>G
|
|
|
ENST00000596548.1:c.16C>G
|
ENSP00000469744.1:p.His6Asp
|
|
ENST00000601008.1:c.241+1723C>G
|
ENSP00000471384.1:n.241+1723C>G
|
|
NM_000064.3:c.3934C>G
|
NP_000055.2:p.His1312Asp
|
|
NM_000064.4:c.3934C>G
MANE Select
|
NP_000055.2:p.His1312Asp
|
|