ENST00000318471.5:c.328C>G
MANE Select
|
ENSP00000315680.3:p.His110Asp
|
|
ENST00000541292.6:c.328C>G
|
ENSP00000441004.1:p.His110Asp
|
|
ENST00000678002.1:c.203C>G
|
|
|
ENST00000678557.1:c.214C>G
|
ENSP00000502962.1:p.His72Asp
|
|
ENST00000678593.1:c.333C>G
|
ENSP00000503841.1:n.333C>G
|
|
ENST00000679286.1:c.208C>G
|
ENSP00000503168.1:p.His70Asp
|
|
ENST00000318471.4:c.328C>G
|
ENSP00000315680.3:p.His110Asp
|
|
ENST00000367756.8:c.328C>G
|
ENSP00000356730.4:p.His110Asp
|
|
ENST00000541292.5:c.328C>G
|
ENSP00000441004.1:p.His110Asp
|
|
NM_000288.3:c.328C>G
|
NP_000279.1:p.His110Asp
|
|
XM_005267019.3:c.214C>G
|
XP_005267076.1:p.His72Asp
|
|
XM_006715502.1:c.328C>G
|
XP_006715565.1:p.His110Asp
|
|
XM_011535900.1:c.328C>G
|
XP_011534202.1:p.His110Asp
|
|
XM_005267019.4:c.214C>G
|
XP_005267076.1:p.His72Asp
|
|
XM_006715502.2:c.328C>G
|
XP_006715565.1:p.His110Asp
|
|
XM_017010934.2:c.328C>G
|
XP_016866423.1:p.His110Asp
|
|
NM_000288.4:c.328C>G
MANE Select
|
NP_000279.1:p.His110Asp
|
|