ENST00000673913.2:c.*226G>C
|
ENSP00000501161.2:n.*226G>C
|
|
ENST00000710286.1:c.2243G>C
|
ENSP00000518176.1:p.Gly748Ala
|
|
ENST00000673903.1:c.1511G>C
|
ENSP00000501257.1:p.Gly504Ala
|
|
ENST00000673913.1:c.736G>C
|
ENSP00000501161.1:n.736G>C
|
|
ENST00000302118.5:c.1886G>C
MANE Select
|
ENSP00000303208.5:p.Gly629Ala
|
|
ENST00000490692.1:n.2432G>C
|
|
|
NM_174936.3:c.1886G>C , LRG_275t1:c.1886G>C
|
NP_777596.2:p.Gly629Ala
|
|
NR_110451.1:n.1493G>C
|
|
|
XM_011541193.1:c.1007G>C
|
XP_011539495.1:p.Gly336Ala
|
|
NM_174936.4:c.1886G>C
MANE Select
|
NP_777596.2:p.Gly629Ala
|
|
NR_110451.2:n.1493G>C
|
|
|