|
NM_018026.4:c.943C>G
MANE Select
|
NP_060496.2:p.Arg315Gly
|
|
ENST00000320580.9:c.943C>G
MANE Select
|
ENSP00000316454.4:p.Arg315Gly
|
|
NM_018026.3:c.943C>G
|
NP_060496.2:p.Arg315Gly
|
|
ENST00000320580.8:c.943C>G
|
ENSP00000316454.4:p.Arg315Gly
|
|
ENST00000524784.1:c.115C>G
|
ENSP00000435037.1:p.Arg39Gly
|
|
ENST00000527224.1:n.1067C>G
|
|
|
ENST00000531298.5:c.204C>G
|
|
|
XM_011545162.1:c.622C>G
|
XP_011543464.1:p.Arg208Gly
|
|
XM_011545163.1:c.613C>G
|
XP_011543465.1:p.Arg205Gly
|
|
XM_011545164.1:c.604C>G
|
XP_011543466.1:p.Arg202Gly
|
|
XM_011545164.2:c.604C>G
|
XP_011543466.1:p.Arg202Gly
|
|
XR_001747924.1:n.1154C>G
|
|