ENST00000695651.1:n.2142G>T
|
|
|
ENST00000695652.1:c.3671G>T
|
ENSP00000512083.1:p.Gly1224Val
|
|
ENST00000695653.1:c.1703G>T
|
ENSP00000512084.1:p.Gly568Val
|
|
ENST00000695654.1:c.2819G>T
|
ENSP00000512085.1:p.Gly940Val
|
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ENST00000695655.1:c.2735G>T
|
ENSP00000512086.1:n.2735G>T
|
|
ENST00000695692.1:n.3158G>T
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|
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ENST00000245907.11:c.3794G>T
MANE Select
|
ENSP00000245907.4:p.Gly1265Val
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|
ENST00000245907.10:c.3794G>T
|
ENSP00000245907.4:p.Gly1265Val
|
|
ENST00000596238.1:n.237G>T
|
|
|
ENST00000601008.1:c.241+606G>T
|
ENSP00000471384.1:n.241+606G>T
|
|
NM_000064.3:c.3794G>T
|
NP_000055.2:p.Gly1265Val
|
|
NM_000064.4:c.3794G>T
MANE Select
|
NP_000055.2:p.Gly1265Val
|
|