ENST00000695666.1:n.893G>A
|
|
|
ENST00000695667.1:n.411G>A
|
|
|
ENST00000695668.1:n.2391G>A
|
|
|
ENST00000300692.9:c.406G>A
MANE Select
|
ENSP00000300692.4:p.Ala136Thr
|
|
ENST00000300692.8:c.406G>A
|
ENSP00000300692.4:p.Ala136Thr
|
|
ENST00000392884.2:c.275-281G>A
|
ENSP00000376622.2:n.275-281G>A
|
|
ENST00000526561.1:n.80-281G>A
|
|
|
ENST00000529594.5:c.187G>A
|
ENSP00000437335.1:p.Ala63Thr
|
|
ENST00000534687.5:c.288-281G>A
|
|
|
NM_000732.4:c.406G>A , LRG_37t1:c.406G>A
|
NP_000723.1:p.Ala136Thr
|
|
NM_001040651.1:c.275-281G>A
|
NP_001035741.1:n.275-281G>A
|
|
NM_001040651.2:c.275-281G>A
|
NP_001035741.1:n.275-281G>A
|
|
NM_000732.6:c.406G>A
MANE Select
|
NP_000723.1:p.Ala136Thr
|
|