ENST00000697149.1:c.1429T>C
|
ENSP00000513138.1:n.1429T>C
|
|
ENST00000697150.1:c.1487T>C
|
ENSP00000513139.1:n.1487T>C
|
|
ENST00000697151.1:c.1420T>C
|
ENSP00000513140.1:n.1420T>C
|
|
ENST00000697164.1:c.1500T>C
|
ENSP00000513153.1:p.Phe500=
|
|
ENST00000697165.1:c.1287T>C
|
ENSP00000513154.1:p.Phe429=
|
|
ENST00000347310.10:c.1590T>C
MANE Select
|
ENSP00000321345.5:p.Phe530=
|
|
ENST00000637002.1:c.981T>C
|
ENSP00000490340.1:p.Phe327=
|
|
ENST00000347310.9:c.1590T>C
|
ENSP00000321345.5:p.Phe530=
|
|
ENST00000395227.2:c.384T>C
|
ENSP00000378652.2:p.Phe128=
|
|
ENST00000425614.3:c.825T>C
|
ENSP00000387640.2:p.Phe275=
|
|
ENST00000473881.2:c.*416T>C
|
ENSP00000486667.1:n.*416T>C
|
|
NM_144701.2:c.1590T>C
|
NP_653302.2:p.Phe530=
|
|
XM_005270516.2:c.828T>C
|
XP_005270573.1:p.Phe276=
|
|
XM_011540789.1:c.1680T>C
|
XP_011539091.1:p.Phe560=
|
|
XM_011540790.1:c.1590T>C
|
XP_011539092.1:p.Phe530=
|
|
XM_011540791.1:c.1590T>C
|
XP_011539093.1:p.Phe530=
|
|
XM_011540790.3:c.1590T>C
|
XP_011539092.1:p.Phe530=
|
|
XM_011540791.3:c.1590T>C
|
XP_011539093.1:p.Phe530=
|
|
XR_001736993.1:n.1670T>C
|
|
|
NM_144701.3:c.1590T>C
MANE Select
|
NP_653302.2:p.Phe530=
|
|