ENST00000327892.13:c.753C>A
MANE Select
|
ENSP00000339001.7:p.Arg251=
|
|
ENST00000680530.1:n.1615C>A
|
|
|
ENST00000681421.1:n.1819C>A
|
|
|
ENST00000681435.1:c.537C>A
|
ENSP00000506665.1:p.Arg179=
|
|
ENST00000327892.12:c.753C>A
|
ENSP00000339001.7:p.Arg251=
|
|
ENST00000330914.7:c.537C>A
|
ENSP00000365578.2:p.Arg179=
|
|
ENST00000396384.1:c.537C>A
|
ENSP00000379668.1:p.Arg179=
|
|
ENST00000396389.5:c.699C>A
|
ENSP00000379672.1:p.Arg233=
|
|
NM_001293212.1:c.813C>A
|
NP_001280141.1:p.Arg271=
|
|
NM_001293213.1:c.370-223C>A
|
NP_001280142.1:n.370-223C>A
|
|
NM_001293214.1:c.621C>A
|
NP_001280143.1:p.Arg207=
|
|
NM_001293215.1:c.537C>A
|
NP_001280144.1:p.Arg179=
|
|
NM_001293216.1:c.537C>A
|
NP_001280145.1:p.Arg179=
|
|
NM_178014.3:c.753C>A
|
NP_821133.1:p.Arg251=
|
|
NR_120608.1:n.584-124C>A
|
|
|
NM_178014.4:c.753C>A
MANE Select
|
NP_821133.1:p.Arg251=
|
|
NM_001293212.2:c.813C>A
|
NP_001280141.1:p.Arg271=
|
|
NM_001293213.2:c.370-223C>A
|
NP_001280142.1:n.370-223C>A
|
|
NM_001293214.2:c.621C>A
|
NP_001280143.1:p.Arg207=
|
|
NM_001293215.2:c.537C>A
|
NP_001280144.1:p.Arg179=
|
|
NM_001293216.2:c.537C>A
|
NP_001280145.1:p.Arg179=
|
|
NR_120608.2:n.433-124C>A
|
|
|