ENST00000436784.7:c.1547A>C
MANE Select
|
ENSP00000389175.2:p.His516Pro
|
|
ENST00000436784.6:c.1547A>C
|
ENSP00000389175.2:p.His516Pro
|
|
ENST00000461183.5:c.819A>C
|
ENSP00000417264.1:p.Pro273=
|
|
ENST00000471180.5:c.690A>C
|
ENSP00000417526.1:p.Pro230=
|
|
ENST00000473032.5:c.585A>C
|
ENSP00000418951.1:p.Pro195=
|
|
ENST00000486393.5:c.*910A>C
|
ENSP00000419868.1:n.*910A>C
|
|
ENST00000489173.1:n.1841A>C
|
|
|
NM_145262.3:c.1547A>C
|
NP_660305.2:p.His516Pro
|
|
NR_026699.1:n.1645A>C
|
|
|
NR_026700.1:n.751A>C
|
|
|
NR_026701.1:n.1643A>C
|
|
|
NR_026702.1:n.681A>C
|
|
|
XM_005264878.2:c.*666A>C
|
XP_005264935.1:n.*666A>C
|
|
XR_245095.2:n.2798A>C
|
|
|
XM_017005730.1:c.1166A>C
|
XP_016861219.1:p.His389Pro
|
|
XM_024453351.1:c.1547A>C
|
XP_024309119.1:p.His516Pro
|
|
XM_024453352.1:c.*666A>C
|
XP_024309120.1:n.*666A>C
|
|
XR_001740022.2:n.3449A>C
|
|
|
XR_001740023.2:n.2973A>C
|
|
|
XR_245095.4:n.2799A>C
|
|
|
NM_145262.4:c.1547A>C
MANE Select
|
NP_660305.2:p.His516Pro
|
|
NR_026699.2:n.1637A>C
|
|
|
NR_026700.2:n.743A>C
|
|
|
NR_026701.2:n.1635A>C
|
|
|
NR_026702.2:n.673A>C
|
|
|
NM_001144951.2:c.*666A>C
|
NP_001138423.1:n.*666A>C
|
|