ENST00000262367.10:c.6918G>C
MANE Select
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ENSP00000262367.5:p.Gly2306=
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ENST00000262367.9:c.6918G>C
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ENSP00000262367.5:p.Gly2306=
|
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ENST00000382070.7:c.6804G>C
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ENSP00000371502.3:p.Gly2268=
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NM_001079846.1:c.6804G>C
|
NP_001073315.1:p.Gly2268=
|
|
NM_004380.2:c.6918G>C
|
NP_004371.2:p.Gly2306=
|
|
XM_005255124.3:c.6873G>C
|
XP_005255181.1:p.Gly2291=
|
|
XM_005255125.3:c.6501G>C
|
XP_005255182.1:p.Gly2167=
|
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XM_006720848.2:c.6657G>C
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XP_006720911.1:p.Gly2219=
|
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XM_011522380.1:c.6864G>C
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XP_011520682.1:p.Gly2288=
|
|
XM_011522381.1:c.6165G>C
|
XP_011520683.1:p.Gly2055=
|
|
XM_005255124.4:c.6873G>C
|
XP_005255181.1:p.Gly2291=
|
|
XM_005255125.4:c.6501G>C
|
XP_005255182.1:p.Gly2167=
|
|
XM_006720848.3:c.6657G>C
|
XP_006720911.1:p.Gly2219=
|
|
XM_011522381.2:c.6165G>C
|
XP_011520683.1:p.Gly2055=
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XM_017022944.1:c.6912G>C
|
XP_016878433.1:p.Gly2304=
|
|
NM_004380.3:c.6918G>C
MANE Select
|
NP_004371.2:p.Gly2306=
|
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