ENST00000436784.7:c.1569G>T
MANE Select
|
ENSP00000389175.2:p.Arg523=
|
|
ENST00000436784.6:c.1569G>T
|
ENSP00000389175.2:p.Arg523=
|
|
ENST00000461183.5:c.841G>T
|
ENSP00000417264.1:p.Val281Leu
|
|
ENST00000471180.5:c.712G>T
|
ENSP00000417526.1:p.Val238Leu
|
|
ENST00000473032.5:c.607G>T
|
ENSP00000418951.1:p.Val203Leu
|
|
ENST00000486393.5:c.*932G>T
|
ENSP00000419868.1:n.*932G>T
|
|
ENST00000489173.1:n.1863G>T
|
|
|
NM_145262.3:c.1569G>T
|
NP_660305.2:p.Arg523=
|
|
NR_026699.1:n.1667G>T
|
|
|
NR_026700.1:n.773G>T
|
|
|
NR_026701.1:n.1665G>T
|
|
|
NR_026702.1:n.703G>T
|
|
|
XM_005264878.2:c.*688G>T
|
XP_005264935.1:n.*688G>T
|
|
XR_245095.2:n.2820G>T
|
|
|
XM_017005730.1:c.1188G>T
|
XP_016861219.1:p.Arg396=
|
|
XM_024453351.1:c.1569G>T
|
XP_024309119.1:p.Arg523=
|
|
XM_024453352.1:c.*688G>T
|
XP_024309120.1:n.*688G>T
|
|
XR_001740022.2:n.3471G>T
|
|
|
XR_001740023.2:n.2995G>T
|
|
|
XR_245095.4:n.2821G>T
|
|
|
NM_145262.4:c.1569G>T
MANE Select
|
NP_660305.2:p.Arg523=
|
|
NR_026699.2:n.1659G>T
|
|
|
NR_026700.2:n.765G>T
|
|
|
NR_026701.2:n.1657G>T
|
|
|
NR_026702.2:n.695G>T
|
|
|
NM_001144951.2:c.*688G>T
|
NP_001138423.1:n.*688G>T
|
|