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MANE Select
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ENSP00000262367.5:p.Arg1202=
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ENST00000262367.9:c.3605G=
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ENSP00000262367.5:p.Arg1202=
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ENST00000382070.7:c.3491G=
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ENSP00000371502.3:p.Arg1164=
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ENST00000570939.2:c.2210G=
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ENSP00000461002.2:p.Arg737=
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NM_001079846.1:c.3491G=
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NP_001073315.1:p.Arg1164=
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NM_004380.2:c.3605G=
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NP_004371.2:p.Arg1202=
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XM_005255124.3:c.3560G=
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XP_005255181.1:p.Arg1187=
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XM_005255125.3:c.3188G=
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XP_005255182.1:p.Arg1063=
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XM_006720848.2:c.3605G=
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XP_006720911.1:p.Arg1202=
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XM_011522380.1:c.3551G=
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XP_011520682.1:p.Arg1184=
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XM_011522381.1:c.2852G=
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XP_011520683.1:p.Arg951=
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XM_011522382.1:c.3605G=
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XP_011520684.1:p.Arg1202=
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XM_005255124.4:c.3560G=
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XP_005255181.1:p.Arg1187=
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XM_005255125.4:c.3188G=
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XP_005255182.1:p.Arg1063=
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XM_006720848.3:c.3605G=
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XP_006720911.1:p.Arg1202=
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XM_011522381.2:c.2852G=
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XP_011520683.1:p.Arg951=
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XM_011522382.3:c.3605G=
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XP_011520684.1:p.Arg1202=
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XM_017022944.1:c.3599G=
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XP_016878433.1:p.Arg1200=
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NM_004380.3:c.3605G=
MANE Select
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NP_004371.2:p.Arg1202=
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