ENST00000262367.10:c.6197C>G
MANE Select
|
ENSP00000262367.5:p.Ala2066Gly
|
|
ENST00000262367.9:c.6197C>G
|
ENSP00000262367.5:p.Ala2066Gly
|
|
ENST00000382070.7:c.6083C>G
|
ENSP00000371502.3:p.Ala2028Gly
|
|
NM_001079846.1:c.6083C>G
|
NP_001073315.1:p.Ala2028Gly
|
|
NM_004380.2:c.6197C>G
|
NP_004371.2:p.Ala2066Gly
|
|
XM_005255124.3:c.6152C>G
|
XP_005255181.1:p.Ala2051Gly
|
|
XM_005255125.3:c.5780C>G
|
XP_005255182.1:p.Ala1927Gly
|
|
XM_006720848.2:c.5936C>G
|
XP_006720911.1:p.Ala1979Gly
|
|
XM_011522380.1:c.6143C>G
|
XP_011520682.1:p.Ala2048Gly
|
|
XM_011522381.1:c.5444C>G
|
XP_011520683.1:p.Ala1815Gly
|
|
XM_005255124.4:c.6152C>G
|
XP_005255181.1:p.Ala2051Gly
|
|
XM_005255125.4:c.5780C>G
|
XP_005255182.1:p.Ala1927Gly
|
|
XM_006720848.3:c.5936C>G
|
XP_006720911.1:p.Ala1979Gly
|
|
XM_011522381.2:c.5444C>G
|
XP_011520683.1:p.Ala1815Gly
|
|
XM_017022944.1:c.6191C>G
|
XP_016878433.1:p.Ala2064Gly
|
|
NM_004380.3:c.6197C>G
MANE Select
|
NP_004371.2:p.Ala2066Gly
|
|