ENST00000221930.6:c.507G>T
MANE Select
|
ENSP00000221930.4:p.Glu169Asp
|
|
ENST00000600196.2:c.507G>T
|
ENSP00000504008.1:p.Glu169Asp
|
|
ENST00000677934.1:c.507G>T
|
ENSP00000504769.1:p.Glu169Asp
|
|
ENST00000221930.5:c.507G>T
|
ENSP00000221930.4:p.Glu169Asp
|
|
ENST00000597453.1:n.38G>T
|
|
|
NM_000660.5:c.507G>T
|
NP_000651.3:p.Glu169Asp
|
|
XM_011527242.1:c.507G>T
|
XP_011525544.1:p.Glu169Asp
|
|
NM_000660.6:c.507G>T
|
NP_000651.3:p.Glu169Asp
|
|
XM_011527242.2:c.507G>T
|
XP_011525544.1:p.Glu169Asp
|
|
NM_000660.7:c.507G>T
MANE Select
|
NP_000651.3:p.Glu169Asp
|
|