ENST00000695651.1:n.2186G>A
|
|
|
ENST00000695653.1:c.1747G>A
|
ENSP00000512084.1:p.Ala583Thr
|
|
ENST00000695654.1:c.2863G>A
|
ENSP00000512085.1:p.Ala955Thr
|
|
ENST00000695690.1:n.29G>A
|
|
|
ENST00000695691.1:n.29G>A
|
|
|
ENST00000245907.11:c.3838G>A
MANE Select
|
ENSP00000245907.4:p.Ala1280Thr
|
|
ENST00000245907.10:c.3838G>A
|
ENSP00000245907.4:p.Ala1280Thr
|
|
ENST00000596238.1:n.281G>A
|
|
|
ENST00000601008.1:c.241+1627G>A
|
ENSP00000471384.1:n.241+1627G>A
|
|
NM_000064.3:c.3838G>A
|
NP_000055.2:p.Ala1280Thr
|
|
NM_000064.4:c.3838G>A
MANE Select
|
NP_000055.2:p.Ala1280Thr
|
|