ENST00000695651.1:n.2142G>A
|
|
|
ENST00000695652.1:c.3671G>A
|
ENSP00000512083.1:p.Gly1224Asp
|
|
ENST00000695653.1:c.1703G>A
|
ENSP00000512084.1:p.Gly568Asp
|
|
ENST00000695654.1:c.2819G>A
|
ENSP00000512085.1:p.Gly940Asp
|
|
ENST00000695655.1:c.2735G>A
|
ENSP00000512086.1:n.2735G>A
|
|
ENST00000695692.1:n.3158G>A
|
|
|
ENST00000245907.11:c.3794G>A
MANE Select
|
ENSP00000245907.4:p.Gly1265Asp
|
|
ENST00000245907.10:c.3794G>A
|
ENSP00000245907.4:p.Gly1265Asp
|
|
ENST00000596238.1:n.237G>A
|
|
|
ENST00000601008.1:c.241+606G>A
|
ENSP00000471384.1:n.241+606G>A
|
|
NM_000064.3:c.3794G>A
|
NP_000055.2:p.Gly1265Asp
|
|
NM_000064.4:c.3794G>A
MANE Select
|
NP_000055.2:p.Gly1265Asp
|
|