ENST00000255078.8:c.1518A>C
MANE Select
|
ENSP00000255078.4:p.Glu506Asp
|
|
ENST00000674955.1:c.*235A>C
|
ENSP00000502463.1:n.*235A>C
|
|
ENST00000675118.1:c.1006A>C
|
|
|
ENST00000675205.1:n.183+413A>C
|
|
|
ENST00000675615.1:c.1518A>C
|
ENSP00000502413.1:p.Glu506Asp
|
|
ENST00000675648.1:n.893A>C
|
|
|
ENST00000675997.1:n.113-570A>C
|
|
|
ENST00000676173.1:n.2263A>C
|
|
|
ENST00000676228.1:c.*841A>C
|
ENSP00000502375.1:n.*841A>C
|
|
ENST00000255078.7:c.1518A>C
|
ENSP00000255078.3:p.Glu506Asp
|
|
ENST00000537458.5:n.635A>C
|
|
|
ENST00000539064.5:n.1277A>C
|
|
|
ENST00000541229.5:n.213A>C
|
|
|
ENST00000543739.5:n.635A>C
|
|
|
NM_002180.2:c.1518A>C , LRG_250t1:c.1518A>C
|
NP_002171.2:p.Glu506Asp
|
|
XM_005273974.2:c.507A>C
|
XP_005274031.1:p.Glu169Asp
|
|
XM_005273975.2:c.390A>C
|
XP_005274032.1:p.Glu130Asp
|
|
XM_011544994.1:c.285A>C
|
XP_011543296.1:p.Glu95Asp
|
|
XR_949903.1:n.1620A>C
|
|
|
XM_005273975.3:c.390A>C
|
XP_005274032.1:p.Glu130Asp
|
|
XM_017017669.2:c.507A>C
|
XP_016873158.1:p.Glu169Asp
|
|
XM_017017670.2:c.507A>C
|
XP_016873159.1:p.Glu169Asp
|
|
XM_017017671.2:c.1518A>C
|
XP_016873160.1:p.Glu506Asp
|
|
XR_949903.3:n.1616A>C
|
|
|
NM_002180.3:c.1518A>C
MANE Select
|
NP_002171.2:p.Glu506Asp
|
|