ENST00000697149.1:c.1703A>C
|
ENSP00000513138.1:n.1703A>C
|
|
ENST00000697150.1:c.1761A>C
|
ENSP00000513139.1:n.1761A>C
|
|
ENST00000697151.1:c.1694A>C
|
ENSP00000513140.1:n.1694A>C
|
|
ENST00000697164.1:c.1774A>C
|
ENSP00000513153.1:p.Asn592His
|
|
ENST00000697165.1:c.1561A>C
|
ENSP00000513154.1:p.Asn521His
|
|
ENST00000347310.10:c.1864A>C
MANE Select
|
ENSP00000321345.5:p.Asn622His
|
|
ENST00000637002.1:c.1255A>C
|
ENSP00000490340.1:p.Asn419His
|
|
ENST00000347310.9:c.1864A>C
|
ENSP00000321345.5:p.Asn622His
|
|
ENST00000395227.2:c.658A>C
|
ENSP00000378652.2:p.Asn220His
|
|
ENST00000425614.3:c.1099A>C
|
ENSP00000387640.2:p.Asn367His
|
|
ENST00000473881.2:c.*690A>C
|
ENSP00000486667.1:n.*690A>C
|
|
NM_144701.2:c.1864A>C
|
NP_653302.2:p.Asn622His
|
|
XM_005270516.2:c.1102A>C
|
XP_005270573.1:p.Asn368His
|
|
XM_011540789.1:c.1954A>C
|
XP_011539091.1:p.Asn652His
|
|
XM_011540790.1:c.1864A>C
|
XP_011539092.1:p.Asn622His
|
|
XM_011540791.1:c.1864A>C
|
XP_011539093.1:p.Asn622His
|
|
XM_011540790.3:c.1864A>C
|
XP_011539092.1:p.Asn622His
|
|
XM_011540791.3:c.1864A>C
|
XP_011539093.1:p.Asn622His
|
|
XR_001736993.1:n.1944A>C
|
|
|
NM_144701.3:c.1864A>C
MANE Select
|
NP_653302.2:p.Asn622His
|
|