ENST00000697149.1:c.1464A>C
|
ENSP00000513138.1:n.1464A>C
|
|
ENST00000697150.1:c.1522A>C
|
ENSP00000513139.1:n.1522A>C
|
|
ENST00000697151.1:c.1455A>C
|
ENSP00000513140.1:n.1455A>C
|
|
ENST00000697164.1:c.1535A>C
|
ENSP00000513153.1:p.Asn512Thr
|
|
ENST00000697165.1:c.1322A>C
|
ENSP00000513154.1:p.Asn441Thr
|
|
ENST00000347310.10:c.1625A>C
MANE Select
|
ENSP00000321345.5:p.Asn542Thr
|
|
ENST00000637002.1:c.1016A>C
|
ENSP00000490340.1:p.Asn339Thr
|
|
ENST00000347310.9:c.1625A>C
|
ENSP00000321345.5:p.Asn542Thr
|
|
ENST00000395227.2:c.419A>C
|
ENSP00000378652.2:p.Asn140Thr
|
|
ENST00000425614.3:c.860A>C
|
ENSP00000387640.2:p.Asn287Thr
|
|
ENST00000473881.2:c.*451A>C
|
ENSP00000486667.1:n.*451A>C
|
|
NM_144701.2:c.1625A>C
|
NP_653302.2:p.Asn542Thr
|
|
XM_005270516.2:c.863A>C
|
XP_005270573.1:p.Asn288Thr
|
|
XM_011540789.1:c.1715A>C
|
XP_011539091.1:p.Asn572Thr
|
|
XM_011540790.1:c.1625A>C
|
XP_011539092.1:p.Asn542Thr
|
|
XM_011540791.1:c.1625A>C
|
XP_011539093.1:p.Asn542Thr
|
|
XM_011540790.3:c.1625A>C
|
XP_011539092.1:p.Asn542Thr
|
|
XM_011540791.3:c.1625A>C
|
XP_011539093.1:p.Asn542Thr
|
|
XR_001736993.1:n.1705A>C
|
|
|
NM_144701.3:c.1625A>C
MANE Select
|
NP_653302.2:p.Asn542Thr
|
|