ENST00000673913.2:c.*97A>C
|
ENSP00000501161.2:n.*97A>C
|
|
ENST00000710286.1:c.2114A>C
|
ENSP00000518176.1:p.Asn705Thr
|
|
ENST00000673903.1:c.1382A>C
|
ENSP00000501257.1:p.Asn461Thr
|
|
ENST00000673913.1:c.607A>C
|
ENSP00000501161.1:n.607A>C
|
|
ENST00000302118.5:c.1757A>C
MANE Select
|
ENSP00000303208.5:p.Asn586Thr
|
|
ENST00000490692.1:n.2303A>C
|
|
|
NM_174936.3:c.1757A>C , LRG_275t1:c.1757A>C
|
NP_777596.2:p.Asn586Thr
|
|
NR_110451.1:n.1364A>C
|
|
|
XM_011541193.1:c.878A>C
|
XP_011539495.1:p.Asn293Thr
|
|
NM_174936.4:c.1757A>C
MANE Select
|
NP_777596.2:p.Asn586Thr
|
|
NR_110451.2:n.1364A>C
|
|
|