ENST00000262367.10:c.6131C>G
MANE Select
|
ENSP00000262367.5:p.Ala2044Gly
|
|
ENST00000262367.9:c.6131C>G
|
ENSP00000262367.5:p.Ala2044Gly
|
|
ENST00000382070.7:c.6017C>G
|
ENSP00000371502.3:p.Ala2006Gly
|
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NM_001079846.1:c.6017C>G
|
NP_001073315.1:p.Ala2006Gly
|
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NM_004380.2:c.6131C>G
|
NP_004371.2:p.Ala2044Gly
|
|
XM_005255124.3:c.6086C>G
|
XP_005255181.1:p.Ala2029Gly
|
|
XM_005255125.3:c.5714C>G
|
XP_005255182.1:p.Ala1905Gly
|
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XM_006720848.2:c.5870C>G
|
XP_006720911.1:p.Ala1957Gly
|
|
XM_011522380.1:c.6077C>G
|
XP_011520682.1:p.Ala2026Gly
|
|
XM_011522381.1:c.5378C>G
|
XP_011520683.1:p.Ala1793Gly
|
|
XM_005255124.4:c.6086C>G
|
XP_005255181.1:p.Ala2029Gly
|
|
XM_005255125.4:c.5714C>G
|
XP_005255182.1:p.Ala1905Gly
|
|
XM_006720848.3:c.5870C>G
|
XP_006720911.1:p.Ala1957Gly
|
|
XM_011522381.2:c.5378C>G
|
XP_011520683.1:p.Ala1793Gly
|
|
XM_017022944.1:c.6125C>G
|
XP_016878433.1:p.Ala2042Gly
|
|
NM_004380.3:c.6131C>G
MANE Select
|
NP_004371.2:p.Ala2044Gly
|
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