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ENST00000648388.1:c.976C=
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ENST00000649156.2:c.976C=
MANE Select
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ENSP00000497871.1:p.Arg304=
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ENSP00000506293.1:n.*495C=
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NM_172250.2:c.976C=
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XM_011531684.1:c.976C=
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XP_011529986.1:p.Arg326=
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XM_011531685.1:c.976C=
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XP_011529987.1:p.Arg326=
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XM_011531686.1:c.481C=
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XP_011529988.1:p.Arg161=
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NM_172250.3:c.976C=
MANE Select
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NP_758454.1:p.Arg326=
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XM_011531684.3:c.976C=
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XP_011529986.1:p.Arg326=
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XM_011531685.2:c.976C=
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XP_011529987.1:p.Arg326=
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XM_011531686.2:c.481C=
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