ENST00000700274.1:c.277C>G
|
ENSP00000514909.1:p.His93Asp
|
|
ENST00000649276.2:c.751C>G
MANE Select
|
ENSP00000497003.1:p.His251Asp
|
|
ENST00000329705.11:c.724C>G
|
ENSP00000331176.7:p.His242Asp
|
|
ENST00000332710.8:c.724C>G
|
ENSP00000331791.4:p.His242Asp
|
|
ENST00000359500.7:c.724C>G
|
ENSP00000352483.3:p.His242Asp
|
|
ENST00000621939.1:c.724C>G
|
ENSP00000477982.1:p.His242Asp
|
|
NM_005992.1:c.724C>G
|
NP_005983.1:p.His242Asp
|
|
NM_080646.1:c.724C>G
|
NP_542377.1:p.His242Asp
|
|
NM_080647.1:c.724C>G , LRG_226t1:c.724C>G
|
NP_542378.1:p.His242Asp
|
|
XM_006724312.1:c.724C>G
|
XP_006724375.1:p.His242Asp
|
|
XM_011530351.1:c.751C>G
|
XP_011528653.1:p.His251Asp
|
|
XM_006724312.2:c.724C>G
|
XP_006724375.1:p.His242Asp
|
|
XM_017028925.1:c.874C>G
|
XP_016884414.1:p.His292Asp
|
|
XM_017028926.1:c.724C>G
|
XP_016884415.1:p.His242Asp
|
|
XM_017028927.1:c.25C>G
|
XP_016884416.1:p.His9Asp
|
|
XM_017028928.1:c.874C>G
|
XP_016884417.1:p.His292Asp
|
|
NM_001379200.1:c.751C>G
MANE Select
|
NP_001366129.1:p.His251Asp
|
|
NM_080646.2:c.724C>G
|
NP_542377.1:p.His242Asp
|
|