ENST00000334785.12:c.*73G>A
MANE Select
|
ENSP00000333938.7:n.*73G>A
|
|
ENST00000330010.12:c.*73G>A
|
ENSP00000327363.8:n.*73G>A
|
|
ENST00000334785.11:c.*73G>A
|
ENSP00000333938.7:n.*73G>A
|
|
ENST00000342754.5:c.1719G>A
|
|
|
ENST00000480732.2:n.1675G>A
|
|
|
NM_001172309.1:c.*73G>A
|
NP_001165780.1:n.*73G>A
|
|
NM_144573.3:c.*73G>A , LRG_442t1:c.*73G>A
|
NP_653174.3:n.*73G>A
|
|
XM_005271322.2:c.2020G>A
|
XP_005271379.1:p.Asp674Asn
|
|
XM_005271323.2:c.1978G>A
|
XP_005271380.1:p.Asp660Asn
|
|
XM_005271324.3:c.1828G>A
|
XP_005271381.1:p.Asp610Asn
|
|
XM_005271325.2:c.1798G>A
|
XP_005271382.1:p.Asp600Asn
|
|
XM_005271326.2:c.1786G>A
|
XP_005271383.1:p.Asp596Asn
|
|
XM_005271327.2:c.1603G>A
|
XP_005271384.1:p.Asp535Asn
|
|
XM_005271322.4:c.2020G>A
|
XP_005271379.1:p.Asp674Asn
|
|
XM_005271323.4:c.1978G>A
|
XP_005271380.1:p.Asp660Asn
|
|
XM_005271324.5:c.1828G>A
|
XP_005271381.1:p.Asp610Asn
|
|
XM_005271325.4:c.1798G>A
|
XP_005271382.1:p.Asp600Asn
|
|
XM_005271326.4:c.1786G>A
|
XP_005271383.1:p.Asp596Asn
|
|
XM_005271327.4:c.1603G>A
|
XP_005271384.1:p.Asp535Asn
|
|
NM_001172309.2:c.*73G>A
|
NP_001165780.1:n.*73G>A
|
|
NM_144573.4:c.*73G>A
MANE Select
|
NP_653174.3:n.*73G>A
|
|