ENST00000695651.1:n.985G>T
|
|
|
ENST00000695652.1:c.2514G>T
|
ENSP00000512083.1:p.Lys838Asn
|
|
ENST00000695653.1:c.546G>T
|
ENSP00000512084.1:p.Lys182Asn
|
|
ENST00000695654.1:c.1761G>T
|
ENSP00000512085.1:p.Lys587Asn
|
|
ENST00000695655.1:c.1578G>T
|
ENSP00000512086.1:n.1578G>T
|
|
ENST00000695692.1:n.2001G>T
|
|
|
ENST00000245907.11:c.2637G>T
MANE Select
|
ENSP00000245907.4:p.Lys879Asn
|
|
ENST00000245907.10:c.2637G>T
|
ENSP00000245907.4:p.Lys879Asn
|
|
ENST00000594005.1:n.213G>T
|
|
|
NM_000064.3:c.2637G>T
|
NP_000055.2:p.Lys879Asn
|
|
NM_000064.4:c.2637G>T
MANE Select
|
NP_000055.2:p.Lys879Asn
|
|