ENST00000436784.7:c.1521G>C
MANE Select
|
ENSP00000389175.2:p.Met507Ile
|
|
ENST00000436784.6:c.1521G>C
|
ENSP00000389175.2:p.Met507Ile
|
|
ENST00000461183.5:c.793G>C
|
ENSP00000417264.1:p.Asp265His
|
|
ENST00000471180.5:c.664G>C
|
ENSP00000417526.1:p.Asp222His
|
|
ENST00000473032.5:c.559G>C
|
ENSP00000418951.1:p.Asp187His
|
|
ENST00000486393.5:c.*884G>C
|
ENSP00000419868.1:n.*884G>C
|
|
ENST00000489173.1:n.1815G>C
|
|
|
NM_145262.3:c.1521G>C
|
NP_660305.2:p.Met507Ile
|
|
NR_026699.1:n.1619G>C
|
|
|
NR_026700.1:n.725G>C
|
|
|
NR_026701.1:n.1617G>C
|
|
|
NR_026702.1:n.655G>C
|
|
|
XM_005264878.2:c.*640G>C
|
XP_005264935.1:n.*640G>C
|
|
XR_245095.2:n.2772G>C
|
|
|
XM_017005730.1:c.1140G>C
|
XP_016861219.1:p.Met380Ile
|
|
XM_024453351.1:c.1521G>C
|
XP_024309119.1:p.Met507Ile
|
|
XM_024453352.1:c.*640G>C
|
XP_024309120.1:n.*640G>C
|
|
XR_001740022.2:n.3423G>C
|
|
|
XR_001740023.2:n.2947G>C
|
|
|
XR_245095.4:n.2773G>C
|
|
|
NM_145262.4:c.1521G>C
MANE Select
|
NP_660305.2:p.Met507Ile
|
|
NR_026699.2:n.1611G>C
|
|
|
NR_026700.2:n.717G>C
|
|
|
NR_026701.2:n.1609G>C
|
|
|
NR_026702.2:n.647G>C
|
|
|
NM_001144951.2:c.*640G>C
|
NP_001138423.1:n.*640G>C
|
|