ENST00000299314.12:c.3167A>G
MANE Select
|
ENSP00000299314.7:p.Asn1056Ser
|
|
ENST00000299314.11:c.3167A>G
|
ENSP00000299314.7:p.Asn1056Ser
|
|
ENST00000549194.1:n.33A>G
|
|
|
NM_024312.4:c.3167A>G
|
NP_077288.2:p.Asn1056Ser
|
|
XM_006719593.2:c.3167A>G
|
XP_006719656.1:p.Asn1056Ser
|
|
XM_011538731.1:c.3086A>G
|
XP_011537033.1:p.Asn1029Ser
|
|
XM_006719593.3:c.3167A>G
|
XP_006719656.1:p.Asn1056Ser
|
|
XM_011538731.2:c.3086A>G
|
XP_011537033.1:p.Asn1029Ser
|
|
XM_017019961.1:c.2951A>G
|
XP_016875450.1:p.Asn984Ser
|
|
XM_017019962.2:c.1940A>G
|
XP_016875451.1:p.Asn647Ser
|
|
NM_024312.5:c.3167A>G
MANE Select
|
NP_077288.2:p.Asn1056Ser
|
|