ENST00000262367.10:c.6309G=
MANE Select
|
ENSP00000262367.5:p.Gln2103=
|
|
ENST00000262367.9:c.6309G=
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ENSP00000262367.5:p.Gln2103=
|
|
ENST00000382070.7:c.6195G=
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ENSP00000371502.3:p.Gln2065=
|
|
NM_001079846.1:c.6195G=
|
NP_001073315.1:p.Gln2065=
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|
NM_004380.2:c.6309G=
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NP_004371.2:p.Gln2103=
|
|
XM_005255124.3:c.6264G=
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XP_005255181.1:p.Gln2088=
|
|
XM_005255125.3:c.5892G=
|
XP_005255182.1:p.Gln1964=
|
|
XM_006720848.2:c.6048G=
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XP_006720911.1:p.Gln2016=
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|
XM_011522380.1:c.6255G=
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XP_011520682.1:p.Gln2085=
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|
XM_011522381.1:c.5556G=
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XP_011520683.1:p.Gln1852=
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|
XM_005255124.4:c.6264G=
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XP_005255181.1:p.Gln2088=
|
|
XM_005255125.4:c.5892G=
|
XP_005255182.1:p.Gln1964=
|
|
XM_006720848.3:c.6048G=
|
XP_006720911.1:p.Gln2016=
|
|
XM_011522381.2:c.5556G=
|
XP_011520683.1:p.Gln1852=
|
|
XM_017022944.1:c.6303G=
|
XP_016878433.1:p.Gln2101=
|
|
NM_004380.3:c.6309G=
MANE Select
|
NP_004371.2:p.Gln2103=
|
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