ENST00000697291.1:c.*753C=
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ENSP00000513228.1:n.*753C=
|
|
ENST00000648433.1:c.1156C=
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ENSP00000496816.1:p.Arg386=
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ENST00000649554.1:n.766C=
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|
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ENST00000649979.2:c.1156C=
MANE Select
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ENSP00000497271.1:p.Arg386=
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ENST00000679938.1:c.844C=
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ENSP00000505518.1:p.Arg282=
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ENST00000263642.2:c.1156C=
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ENSP00000263642.2:p.Arg386=
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NM_022168.3:c.1156C=
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NP_071451.2:p.Arg386=
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XM_011511628.1:c.439C=
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XP_011509930.1:p.Arg147=
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XM_011511629.1:c.1156C=
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XP_011509931.1:p.Arg386=
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NM_022168.4:c.1156C=
MANE Select
|
NP_071451.2:p.Arg386=
|
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