ENST00000255078.8:c.1442C>G
MANE Select
|
ENSP00000255078.4:p.Thr481Arg
|
|
ENST00000674955.1:c.*159C>G
|
ENSP00000502463.1:n.*159C>G
|
|
ENST00000675118.1:c.930C>G
|
|
|
ENST00000675205.1:n.183+337C>G
|
|
|
ENST00000675615.1:c.1442C>G
|
ENSP00000502413.1:p.Thr481Arg
|
|
ENST00000675648.1:n.817C>G
|
|
|
ENST00000675997.1:n.113-646C>G
|
|
|
ENST00000676173.1:n.2187C>G
|
|
|
ENST00000676228.1:c.*765C>G
|
ENSP00000502375.1:n.*765C>G
|
|
ENST00000255078.7:c.1442C>G
|
ENSP00000255078.3:p.Thr481Arg
|
|
ENST00000537458.5:n.559C>G
|
|
|
ENST00000539064.5:n.1201C>G
|
|
|
ENST00000541229.5:n.137C>G
|
|
|
ENST00000543739.5:n.559C>G
|
|
|
NM_002180.2:c.1442C>G , LRG_250t1:c.1442C>G
|
NP_002171.2:p.Thr481Arg
|
|
XM_005273974.2:c.431C>G
|
XP_005274031.1:p.Thr144Arg
|
|
XM_005273975.2:c.314C>G
|
XP_005274032.1:p.Thr105Arg
|
|
XM_011544994.1:c.209C>G
|
XP_011543296.1:p.Thr70Arg
|
|
XR_949903.1:n.1544C>G
|
|
|
XM_005273975.3:c.314C>G
|
XP_005274032.1:p.Thr105Arg
|
|
XM_017017669.2:c.431C>G
|
XP_016873158.1:p.Thr144Arg
|
|
XM_017017670.2:c.431C>G
|
XP_016873159.1:p.Thr144Arg
|
|
XM_017017671.2:c.1442C>G
|
XP_016873160.1:p.Thr481Arg
|
|
XR_949903.3:n.1540C>G
|
|
|
NM_002180.3:c.1442C>G
MANE Select
|
NP_002171.2:p.Thr481Arg
|
|