ENST00000697149.1:c.1344A>G
|
ENSP00000513138.1:n.1344A>G
|
|
ENST00000697150.1:c.1402A>G
|
ENSP00000513139.1:n.1402A>G
|
|
ENST00000697151.1:c.1335A>G
|
ENSP00000513140.1:n.1335A>G
|
|
ENST00000697164.1:c.1415A>G
|
ENSP00000513153.1:p.Asn472Ser
|
|
ENST00000697165.1:c.1202A>G
|
ENSP00000513154.1:p.Asn401Ser
|
|
ENST00000347310.10:c.1505A>G
MANE Select
|
ENSP00000321345.5:p.Asn502Ser
|
|
ENST00000637002.1:c.896A>G
|
ENSP00000490340.1:p.Asn299Ser
|
|
ENST00000347310.9:c.1505A>G
|
ENSP00000321345.5:p.Asn502Ser
|
|
ENST00000395227.2:c.299A>G
|
ENSP00000378652.2:p.Asn100Ser
|
|
ENST00000425614.3:c.740A>G
|
ENSP00000387640.2:p.Asn247Ser
|
|
ENST00000473881.2:c.*331A>G
|
ENSP00000486667.1:n.*331A>G
|
|
NM_144701.2:c.1505A>G
|
NP_653302.2:p.Asn502Ser
|
|
XM_005270516.2:c.743A>G
|
XP_005270573.1:p.Asn248Ser
|
|
XM_011540789.1:c.1595A>G
|
XP_011539091.1:p.Asn532Ser
|
|
XM_011540790.1:c.1505A>G
|
XP_011539092.1:p.Asn502Ser
|
|
XM_011540791.1:c.1505A>G
|
XP_011539093.1:p.Asn502Ser
|
|
XM_011540790.3:c.1505A>G
|
XP_011539092.1:p.Asn502Ser
|
|
XM_011540791.3:c.1505A>G
|
XP_011539093.1:p.Asn502Ser
|
|
XR_001736993.1:n.1585A>G
|
|
|
NM_144701.3:c.1505A>G
MANE Select
|
NP_653302.2:p.Asn502Ser
|
|