ENST00000255078.8:c.1535C>A
MANE Select
|
ENSP00000255078.4:p.Pro512His
|
|
ENST00000674955.1:c.*252C>A
|
ENSP00000502463.1:n.*252C>A
|
|
ENST00000675118.1:c.1023C>A
|
|
|
ENST00000675205.1:n.183+430C>A
|
|
|
ENST00000675615.1:c.1535C>A
|
ENSP00000502413.1:p.Pro512His
|
|
ENST00000675648.1:n.910C>A
|
|
|
ENST00000675997.1:n.113-553C>A
|
|
|
ENST00000676173.1:n.2280C>A
|
|
|
ENST00000676228.1:c.*858C>A
|
ENSP00000502375.1:n.*858C>A
|
|
ENST00000255078.7:c.1535C>A
|
ENSP00000255078.3:p.Pro512His
|
|
ENST00000537458.5:n.652C>A
|
|
|
ENST00000539064.5:n.1294C>A
|
|
|
ENST00000541229.5:n.230C>A
|
|
|
ENST00000543739.5:n.652C>A
|
|
|
NM_002180.2:c.1535C>A , LRG_250t1:c.1535C>A
|
NP_002171.2:p.Pro512His
|
|
XM_005273974.2:c.524C>A
|
XP_005274031.1:p.Pro175His
|
|
XM_005273975.2:c.407C>A
|
XP_005274032.1:p.Pro136His
|
|
XM_011544994.1:c.302C>A
|
XP_011543296.1:p.Pro101His
|
|
XR_949903.1:n.1637C>A
|
|
|
XM_005273975.3:c.407C>A
|
XP_005274032.1:p.Pro136His
|
|
XM_017017669.2:c.524C>A
|
XP_016873158.1:p.Pro175His
|
|
XM_017017670.2:c.524C>A
|
XP_016873159.1:p.Pro175His
|
|
XM_017017671.2:c.1535C>A
|
XP_016873160.1:p.Pro512His
|
|
XR_949903.3:n.1633C>A
|
|
|
NM_002180.3:c.1535C>A
MANE Select
|
NP_002171.2:p.Pro512His
|
|