|
NM_174936.4:c.1274A>G
MANE Select
|
NP_777596.2:p.Asn425Ser
|
|
ENST00000302118.5:c.1274A>G
MANE Select
|
ENSP00000303208.5:p.Asn425Ser
|
|
NM_174936.3:c.1274A>G , LRG_275t1:c.1274A>G
|
NP_777596.2:p.Asn425Ser
|
|
NR_110451.1:n.933A>G
|
|
|
NR_110451.2:n.933A>G
|
|
|
ENST00000490692.1:n.1998A>G
|
|
|
ENST00000673903.1:c.899A>G
|
ENSP00000501257.1:p.Asn300Ser
|
|
ENST00000673913.1:c.14A>G
|
ENSP00000501161.1:p.Asn5Ser
|
|
ENST00000673913.2:c.1274A>G
|
ENSP00000501161.2:p.Asn425Ser
|
|
ENST00000710286.1:c.1631A>G
|
ENSP00000518176.1:p.Asn544Ser
|
|
XM_011541193.1:c.395A>G
|
XP_011539495.1:p.Asn132Ser
|