ENST00000436784.7:c.1279G>T
MANE Select
|
ENSP00000389175.2:p.Ala427Ser
|
|
ENST00000305690.12:c.*398G>T
|
ENSP00000301965.9:n.*398G>T
|
|
ENST00000436784.6:c.1279G>T
|
ENSP00000389175.2:p.Ala427Ser
|
|
ENST00000461183.5:c.764-213G>T
|
ENSP00000417264.1:n.764-213G>T
|
|
ENST00000471180.5:c.635-213G>T
|
ENSP00000417526.1:n.635-213G>T
|
|
ENST00000473032.5:c.530-213G>T
|
ENSP00000418951.1:n.530-213G>T
|
|
ENST00000477382.1:c.*398G>T
|
ENSP00000419008.1:n.*398G>T
|
|
ENST00000486393.5:c.*642G>T
|
ENSP00000419868.1:n.*642G>T
|
|
ENST00000489173.1:n.1573G>T
|
|
|
NM_001144951.1:c.*398G>T
|
NP_001138423.1:n.*398G>T
|
|
NM_145262.3:c.1279G>T
|
NP_660305.2:p.Ala427Ser
|
|
NR_026699.1:n.1377G>T
|
|
|
NR_026700.1:n.696-213G>T
|
|
|
NR_026701.1:n.1375G>T
|
|
|
NR_026702.1:n.626-213G>T
|
|
|
XM_005264878.2:c.*398G>T
|
XP_005264935.1:n.*398G>T
|
|
XR_245095.2:n.2743-213G>T
|
|
|
XM_017005730.1:c.898G>T
|
XP_016861219.1:p.Ala300Ser
|
|
XM_024453351.1:c.1279G>T
|
XP_024309119.1:p.Ala427Ser
|
|
XM_024453352.1:c.*398G>T
|
XP_024309120.1:n.*398G>T
|
|
XR_001740022.2:n.3181G>T
|
|
|
XR_001740023.2:n.2918-213G>T
|
|
|
XR_245095.4:n.2744-213G>T
|
|
|
NM_145262.4:c.1279G>T
MANE Select
|
NP_660305.2:p.Ala427Ser
|
|
NR_026699.2:n.1369G>T
|
|
|
NR_026700.2:n.688-213G>T
|
|
|
NR_026701.2:n.1367G>T
|
|
|
NR_026702.2:n.618-213G>T
|
|
|
NM_001144951.2:c.*398G>T
|
NP_001138423.1:n.*398G>T
|
|