ENST00000436784.7:c.1567C>G
MANE Select
|
ENSP00000389175.2:p.Arg523Gly
|
|
ENST00000436784.6:c.1567C>G
|
ENSP00000389175.2:p.Arg523Gly
|
|
ENST00000461183.5:c.839C>G
|
ENSP00000417264.1:p.Ser280Trp
|
|
ENST00000471180.5:c.710C>G
|
ENSP00000417526.1:p.Ser237Trp
|
|
ENST00000473032.5:c.605C>G
|
ENSP00000418951.1:p.Ser202Trp
|
|
ENST00000486393.5:c.*930C>G
|
ENSP00000419868.1:n.*930C>G
|
|
ENST00000489173.1:n.1861C>G
|
|
|
NM_145262.3:c.1567C>G
|
NP_660305.2:p.Arg523Gly
|
|
NR_026699.1:n.1665C>G
|
|
|
NR_026700.1:n.771C>G
|
|
|
NR_026701.1:n.1663C>G
|
|
|
NR_026702.1:n.701C>G
|
|
|
XM_005264878.2:c.*686C>G
|
XP_005264935.1:n.*686C>G
|
|
XR_245095.2:n.2818C>G
|
|
|
XM_017005730.1:c.1186C>G
|
XP_016861219.1:p.Arg396Gly
|
|
XM_024453351.1:c.1567C>G
|
XP_024309119.1:p.Arg523Gly
|
|
XM_024453352.1:c.*686C>G
|
XP_024309120.1:n.*686C>G
|
|
XR_001740022.2:n.3469C>G
|
|
|
XR_001740023.2:n.2993C>G
|
|
|
XR_245095.4:n.2819C>G
|
|
|
NM_145262.4:c.1567C>G
MANE Select
|
NP_660305.2:p.Arg523Gly
|
|
NR_026699.2:n.1657C>G
|
|
|
NR_026700.2:n.763C>G
|
|
|
NR_026701.2:n.1655C>G
|
|
|
NR_026702.2:n.693C>G
|
|
|
NM_001144951.2:c.*686C>G
|
NP_001138423.1:n.*686C>G
|
|