ENST00000262367.10:c.5388G=
MANE Select
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ENSP00000262367.5:p.Gln1796=
|
|
ENST00000262367.9:c.5388G=
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ENSP00000262367.5:p.Gln1796=
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|
ENST00000382070.7:c.5274G=
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ENSP00000371502.3:p.Gln1758=
|
|
NM_001079846.1:c.5274G=
|
NP_001073315.1:p.Gln1758=
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|
NM_004380.2:c.5388G=
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NP_004371.2:p.Gln1796=
|
|
XM_005255124.3:c.5343G=
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XP_005255181.1:p.Gln1781=
|
|
XM_005255125.3:c.4971G=
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XP_005255182.1:p.Gln1657=
|
|
XM_006720848.2:c.5127G=
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XP_006720911.1:p.Gln1709=
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|
XM_011522380.1:c.5334G=
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XP_011520682.1:p.Gln1778=
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|
XM_011522381.1:c.4635G=
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XP_011520683.1:p.Gln1545=
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|
XM_005255124.4:c.5343G=
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XP_005255181.1:p.Gln1781=
|
|
XM_005255125.4:c.4971G=
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XP_005255182.1:p.Gln1657=
|
|
XM_006720848.3:c.5127G=
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XP_006720911.1:p.Gln1709=
|
|
XM_011522381.2:c.4635G=
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XP_011520683.1:p.Gln1545=
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|
XM_017022944.1:c.5382G=
|
XP_016878433.1:p.Gln1794=
|
|
NM_004380.3:c.5388G=
MANE Select
|
NP_004371.2:p.Gln1796=
|
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