ENST00000673913.2:c.*128C>G
|
ENSP00000501161.2:n.*128C>G
|
|
ENST00000710286.1:c.2145C>G
|
ENSP00000518176.1:p.Ile715Met
|
|
ENST00000673903.1:c.1413C>G
|
ENSP00000501257.1:p.Ile471Met
|
|
ENST00000673913.1:c.638C>G
|
ENSP00000501161.1:n.638C>G
|
|
ENST00000302118.5:c.1788C>G
MANE Select
|
ENSP00000303208.5:p.Ile596Met
|
|
ENST00000490692.1:n.2334C>G
|
|
|
NM_174936.3:c.1788C>G , LRG_275t1:c.1788C>G
|
NP_777596.2:p.Ile596Met
|
|
NR_110451.1:n.1395C>G
|
|
|
XM_011541193.1:c.909C>G
|
XP_011539495.1:p.Ile303Met
|
|
NM_174936.4:c.1788C>G
MANE Select
|
NP_777596.2:p.Ile596Met
|
|
NR_110451.2:n.1395C>G
|
|
|