ENST00000262367.10:c.5216C>G
MANE Select
|
ENSP00000262367.5:p.Ala1739Gly
|
|
ENST00000262367.9:c.5216C>G
|
ENSP00000262367.5:p.Ala1739Gly
|
|
ENST00000382070.7:c.5102C>G
|
ENSP00000371502.3:p.Ala1701Gly
|
|
NM_001079846.1:c.5102C>G
|
NP_001073315.1:p.Ala1701Gly
|
|
NM_004380.2:c.5216C>G
|
NP_004371.2:p.Ala1739Gly
|
|
XM_005255124.3:c.5171C>G
|
XP_005255181.1:p.Ala1724Gly
|
|
XM_005255125.3:c.4799C>G
|
XP_005255182.1:p.Ala1600Gly
|
|
XM_006720848.2:c.4955C>G
|
XP_006720911.1:p.Ala1652Gly
|
|
XM_011522380.1:c.5162C>G
|
XP_011520682.1:p.Ala1721Gly
|
|
XM_011522381.1:c.4463C>G
|
XP_011520683.1:p.Ala1488Gly
|
|
XM_005255124.4:c.5171C>G
|
XP_005255181.1:p.Ala1724Gly
|
|
XM_005255125.4:c.4799C>G
|
XP_005255182.1:p.Ala1600Gly
|
|
XM_006720848.3:c.4955C>G
|
XP_006720911.1:p.Ala1652Gly
|
|
XM_011522381.2:c.4463C>G
|
XP_011520683.1:p.Ala1488Gly
|
|
XM_017022944.1:c.5210C>G
|
XP_016878433.1:p.Ala1737Gly
|
|
NM_004380.3:c.5216C>G
MANE Select
|
NP_004371.2:p.Ala1739Gly
|
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