ENST00000559133.6:c.5058T>A
|
ENSP00000453958.2:p.Asn1686Lys
|
|
ENST00000674301.2:c.5058T>A
|
ENSP00000501333.2:p.Asn1686Lys
|
|
ENST00000684448.1:n.3732T>A
|
|
|
ENST00000316623.10:c.5058T>A
MANE Select
|
ENSP00000325527.5:p.Asn1686Lys
|
|
ENST00000674301.1:c.57T>A
|
ENSP00000501333.1:p.Asn19Lys
|
|
ENST00000316623.9:c.5058T>A
|
ENSP00000325527.5:p.Asn1686Lys
|
|
ENST00000537463.6:c.*821T>A
|
ENSP00000440294.2:n.*821T>A
|
|
ENST00000559133.5:c.365T>A
|
|
|
NM_000138.4:c.5058T>A , LRG_778t1:c.5058T>A
|
NP_000129.3:p.Asn1686Lys
|
|
NM_000138.5:c.5058T>A
MANE Select
|
NP_000129.3:p.Asn1686Lys
|
|