ENST00000647789.2:c.213C=
MANE Select
|
ENSP00000497767.1:p.Asn71=
|
|
ENST00000648064.1:c.213C=
|
ENSP00000497990.1:p.Asn71=
|
|
ENST00000648423.1:c.213C=
|
ENSP00000497985.1:p.Asn71=
|
|
ENST00000648758.1:c.213C=
|
ENSP00000497731.1:p.Asn71=
|
|
ENST00000648906.1:n.383C=
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|
|
ENST00000649902.1:c.213C=
|
ENSP00000497216.1:p.Asn71=
|
|
ENST00000650613.1:n.289C=
|
|
|
ENST00000374855.8:c.213C=
|
ENSP00000363988.4:p.Asn71=
|
|
ENST00000468981.3:n.10C=
|
|
|
ENST00000616752.1:c.213C=
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ENSP00000481363.1:p.Asn71=
|
|
NM_000035.3:c.213C=
|
NP_000026.2:p.Asn71=
|
|
NM_000035.4:c.213C=
MANE Select
|
NP_000026.2:p.Asn71=
|
|