ENST00000322213.9:c.1924G>C
MANE Select
|
ENSP00000323421.3:p.Asp642His
|
|
ENST00000674590.1:c.1156G>C
|
ENSP00000502626.1:p.Asp386His
|
|
ENST00000675065.1:n.1276G>C
|
|
|
ENST00000675504.1:c.1858G>C
|
ENSP00000502524.1:p.Asp620His
|
|
ENST00000322213.8:c.1924G>C
|
ENSP00000323421.3:p.Asp642His
|
|
ENST00000375340.10:c.1858G>C
|
ENSP00000364489.7:p.Asp620His
|
|
NM_001281463.1:c.1858G>C , LRG_773t1:c.1858G>C
|
NP_001268392.1:p.Asp620His
|
|
NM_006306.3:c.1924G>C , LRG_773t2:c.1924G>C
|
NP_006297.2:p.Asp642His
|
|
NM_006306.4:c.1924G>C
MANE Select
|
NP_006297.2:p.Asp642His
|
|