ENST00000673913.2:c.*98C>A
|
ENSP00000501161.2:n.*98C>A
|
|
ENST00000710286.1:c.2115C>A
|
ENSP00000518176.1:p.Asn705Lys
|
|
ENST00000673903.1:c.1383C>A
|
ENSP00000501257.1:p.Asn461Lys
|
|
ENST00000673913.1:c.608C>A
|
ENSP00000501161.1:n.608C>A
|
|
ENST00000302118.5:c.1758C>A
MANE Select
|
ENSP00000303208.5:p.Asn586Lys
|
|
ENST00000490692.1:n.2304C>A
|
|
|
NM_174936.3:c.1758C>A , LRG_275t1:c.1758C>A
|
NP_777596.2:p.Asn586Lys
|
|
NR_110451.1:n.1365C>A
|
|
|
XM_011541193.1:c.879C>A
|
XP_011539495.1:p.Asn293Lys
|
|
NM_174936.4:c.1758C>A
MANE Select
|
NP_777596.2:p.Asn586Lys
|
|
NR_110451.2:n.1365C>A
|
|
|