ENST00000262367.10:c.7040C>G
MANE Select
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ENSP00000262367.5:p.Ala2347Gly
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ENST00000262367.9:c.7040C>G
|
ENSP00000262367.5:p.Ala2347Gly
|
|
ENST00000382070.7:c.6926C>G
|
ENSP00000371502.3:p.Ala2309Gly
|
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NM_001079846.1:c.6926C>G
|
NP_001073315.1:p.Ala2309Gly
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NM_004380.2:c.7040C>G
|
NP_004371.2:p.Ala2347Gly
|
|
XM_005255124.3:c.6995C>G
|
XP_005255181.1:p.Ala2332Gly
|
|
XM_005255125.3:c.6623C>G
|
XP_005255182.1:p.Ala2208Gly
|
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XM_006720848.2:c.6779C>G
|
XP_006720911.1:p.Ala2260Gly
|
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XM_011522380.1:c.6986C>G
|
XP_011520682.1:p.Ala2329Gly
|
|
XM_011522381.1:c.6287C>G
|
XP_011520683.1:p.Ala2096Gly
|
|
XM_005255124.4:c.6995C>G
|
XP_005255181.1:p.Ala2332Gly
|
|
XM_005255125.4:c.6623C>G
|
XP_005255182.1:p.Ala2208Gly
|
|
XM_006720848.3:c.6779C>G
|
XP_006720911.1:p.Ala2260Gly
|
|
XM_011522381.2:c.6287C>G
|
XP_011520683.1:p.Ala2096Gly
|
|
XM_017022944.1:c.7034C>G
|
XP_016878433.1:p.Ala2345Gly
|
|
NM_004380.3:c.7040C>G
MANE Select
|
NP_004371.2:p.Ala2347Gly
|
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