ENST00000436784.7:c.1525G>C
MANE Select
|
ENSP00000389175.2:p.Gly509Arg
|
|
ENST00000436784.6:c.1525G>C
|
ENSP00000389175.2:p.Gly509Arg
|
|
ENST00000461183.5:c.797G>C
|
ENSP00000417264.1:p.Arg266Thr
|
|
ENST00000471180.5:c.668G>C
|
ENSP00000417526.1:p.Arg223Thr
|
|
ENST00000473032.5:c.563G>C
|
ENSP00000418951.1:p.Arg188Thr
|
|
ENST00000486393.5:c.*888G>C
|
ENSP00000419868.1:n.*888G>C
|
|
ENST00000489173.1:n.1819G>C
|
|
|
NM_145262.3:c.1525G>C
|
NP_660305.2:p.Gly509Arg
|
|
NR_026699.1:n.1623G>C
|
|
|
NR_026700.1:n.729G>C
|
|
|
NR_026701.1:n.1621G>C
|
|
|
NR_026702.1:n.659G>C
|
|
|
XM_005264878.2:c.*644G>C
|
XP_005264935.1:n.*644G>C
|
|
XR_245095.2:n.2776G>C
|
|
|
XM_017005730.1:c.1144G>C
|
XP_016861219.1:p.Gly382Arg
|
|
XM_024453351.1:c.1525G>C
|
XP_024309119.1:p.Gly509Arg
|
|
XM_024453352.1:c.*644G>C
|
XP_024309120.1:n.*644G>C
|
|
XR_001740022.2:n.3427G>C
|
|
|
XR_001740023.2:n.2951G>C
|
|
|
XR_245095.4:n.2777G>C
|
|
|
NM_145262.4:c.1525G>C
MANE Select
|
NP_660305.2:p.Gly509Arg
|
|
NR_026699.2:n.1615G>C
|
|
|
NR_026700.2:n.721G>C
|
|
|
NR_026701.2:n.1613G>C
|
|
|
NR_026702.2:n.651G>C
|
|
|
NM_001144951.2:c.*644G>C
|
NP_001138423.1:n.*644G>C
|
|