ENST00000695651.1:n.2035C>A
|
|
|
ENST00000695652.1:c.3564C>A
|
ENSP00000512083.1:p.Asn1188Lys
|
|
ENST00000695653.1:c.1596C>A
|
ENSP00000512084.1:p.Asn532Lys
|
|
ENST00000695654.1:c.2712C>A
|
ENSP00000512085.1:p.Asn904Lys
|
|
ENST00000695655.1:c.2628C>A
|
ENSP00000512086.1:n.2628C>A
|
|
ENST00000695692.1:n.3051C>A
|
|
|
ENST00000245907.11:c.3687C>A
MANE Select
|
ENSP00000245907.4:p.Asn1229Lys
|
|
ENST00000245907.10:c.3687C>A
|
ENSP00000245907.4:p.Asn1229Lys
|
|
ENST00000596238.1:n.130C>A
|
|
|
ENST00000601008.1:c.241+499C>A
|
ENSP00000471384.1:n.241+499C>A
|
|
NM_000064.3:c.3687C>A
|
NP_000055.2:p.Asn1229Lys
|
|
NM_000064.4:c.3687C>A
MANE Select
|
NP_000055.2:p.Asn1229Lys
|
|