ENST00000262493.12:c.771C>G
MANE Select
|
ENSP00000262493.6:p.Asn257Lys
|
|
ENST00000562316.6:c.438C>G
|
ENSP00000457238.2:p.Asn146Lys
|
|
ENST00000564727.2:c.75C>G
|
ENSP00000454971.2:p.Asn25Lys
|
|
ENST00000568375.2:c.116-3435C>G
|
|
|
ENST00000638185.1:n.986C>G
|
|
|
ENST00000638210.1:n.1071C>G
|
|
|
ENST00000638705.1:c.771C>G
|
ENSP00000491223.1:p.Asn257Lys
|
|
ENST00000638836.1:n.681C>G
|
|
|
ENST00000639055.1:n.1492C>G
|
|
|
ENST00000639251.1:n.672C>G
|
|
|
ENST00000639268.1:c.406C>G
|
|
|
ENST00000639341.1:c.296C>G
|
|
|
ENST00000639770.1:c.809C>G
|
ENSP00000491999.1:n.809C>G
|
|
ENST00000640390.1:n.701C>G
|
|
|
ENST00000640469.1:c.135C>G
|
ENSP00000491875.1:p.Asn45Lys
|
|
ENST00000640560.1:n.547C>G
|
|
|
ENST00000640893.1:c.*169C>G
|
ENSP00000492677.1:n.*169C>G
|
|
ENST00000262493.10:c.771C>G
|
ENSP00000262493.6:p.Asn257Lys
|
|
ENST00000568375.1:n.116-3435C>G
|
|
|
NM_020988.2:c.771C>G
|
NP_066268.1:p.Asn257Lys
|
|
XM_011523003.1:c.645C>G
|
XP_011521305.1:p.Asn215Lys
|
|
XM_011523003.3:c.645C>G
|
XP_011521305.1:p.Asn215Lys
|
|
NM_020988.3:c.771C>G
MANE Select
|
NP_066268.1:p.Asn257Lys
|
|