ENST00000682431.1:n.5495G>A
|
|
|
ENST00000682512.1:n.2350G>A
|
|
|
ENST00000682873.1:n.1679G>A
|
|
|
ENST00000683018.1:c.3832G>A
|
ENSP00000506822.1:p.Ala1278Thr
|
|
ENST00000683059.1:c.3832G>A
|
ENSP00000507402.1:p.Ala1278Thr
|
|
ENST00000683142.1:n.1613G>A
|
|
|
ENST00000683164.1:c.3832G>A
|
ENSP00000508051.1:p.Ala1278Thr
|
|
ENST00000683653.1:n.4742G>A
|
|
|
ENST00000684500.1:n.5050G>A
|
|
|
ENST00000684766.1:n.2583G>A
|
|
|
ENST00000267101.8:c.4009G>A
MANE Select
|
ENSP00000267101.4:p.Ala1337Thr
|
|
ENST00000548861.2:c.31+674G>A
|
ENSP00000449770.3:n.31+674G>A
|
|
ENST00000267101.7:c.4009G>A
|
ENSP00000267101.3:p.Ala1337Thr
|
|
ENST00000415288.6:c.3832G>A
|
ENSP00000408340.2:p.Ala1278Thr
|
|
ENST00000548861.1:c.22+674G>A
|
ENSP00000449770.2:n.22+674G>A
|
|
ENST00000549832.1:c.1369G>A
|
ENSP00000448729.1:p.Ala457Thr
|
|
ENST00000550070.6:c.1930G>A
|
ENSP00000448946.2:p.Ala644Thr
|
|
ENST00000551085.5:c.*1426G>A
|
ENSP00000448483.1:n.*1426G>A
|
|
ENST00000551242.5:c.*864G>A
|
ENSP00000447510.1:n.*864G>A
|
|
ENST00000553131.5:c.1732G>A
|
ENSP00000449129.1:p.Ala578Thr
|
|
NM_001982.3:c.4009G>A
|
NP_001973.2:p.Ala1337Thr
|
|
NM_001982.4:c.4009G>A
MANE Select
|
NP_001973.2:p.Ala1337Thr
|
|