ENST00000436784.7:c.1327G>T
MANE Select
|
ENSP00000389175.2:p.Asp443Tyr
|
|
ENST00000305690.12:c.*446G>T
|
ENSP00000301965.9:n.*446G>T
|
|
ENST00000436784.6:c.1327G>T
|
ENSP00000389175.2:p.Asp443Tyr
|
|
ENST00000461183.5:c.764-165G>T
|
ENSP00000417264.1:n.764-165G>T
|
|
ENST00000471180.5:c.635-165G>T
|
ENSP00000417526.1:n.635-165G>T
|
|
ENST00000473032.5:c.530-165G>T
|
ENSP00000418951.1:n.530-165G>T
|
|
ENST00000477382.1:c.*446G>T
|
ENSP00000419008.1:n.*446G>T
|
|
ENST00000486393.5:c.*690G>T
|
ENSP00000419868.1:n.*690G>T
|
|
ENST00000489173.1:n.1621G>T
|
|
|
NM_001144951.1:c.*446G>T
|
NP_001138423.1:n.*446G>T
|
|
NM_145262.3:c.1327G>T
|
NP_660305.2:p.Asp443Tyr
|
|
NR_026699.1:n.1425G>T
|
|
|
NR_026700.1:n.696-165G>T
|
|
|
NR_026701.1:n.1423G>T
|
|
|
NR_026702.1:n.626-165G>T
|
|
|
XM_005264878.2:c.*446G>T
|
XP_005264935.1:n.*446G>T
|
|
XR_245095.2:n.2743-165G>T
|
|
|
XM_017005730.1:c.946G>T
|
XP_016861219.1:p.Asp316Tyr
|
|
XM_024453351.1:c.1327G>T
|
XP_024309119.1:p.Asp443Tyr
|
|
XM_024453352.1:c.*446G>T
|
XP_024309120.1:n.*446G>T
|
|
XR_001740022.2:n.3229G>T
|
|
|
XR_001740023.2:n.2918-165G>T
|
|
|
XR_245095.4:n.2744-165G>T
|
|
|
NM_145262.4:c.1327G>T
MANE Select
|
NP_660305.2:p.Asp443Tyr
|
|
NR_026699.2:n.1417G>T
|
|
|
NR_026700.2:n.688-165G>T
|
|
|
NR_026701.2:n.1415G>T
|
|
|
NR_026702.2:n.618-165G>T
|
|
|
NM_001144951.2:c.*446G>T
|
NP_001138423.1:n.*446G>T
|
|