ENST00000333213.11:c.1486G>C
MANE Select
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ENSP00000327487.6:p.Gly496Arg
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|
ENST00000434205.8:c.1183G>C
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ENSP00000406559.4:p.Gly395Arg
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ENST00000545228.3:c.1674G>C
|
ENSP00000438169.3:p.Val558=
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ENST00000577197.2:n.684G>C
|
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ENST00000579449.2:n.2226G>C
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ENST00000580013.6:n.2630G>C
|
|
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ENST00000679370.1:n.3008G>C
|
|
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ENST00000679429.1:c.*944G>C
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ENSP00000505403.1:n.*944G>C
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ENST00000679443.1:n.1555G>C
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|
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ENST00000679782.1:c.*185G>C
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ENSP00000505995.1:n.*185G>C
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ENST00000679919.1:n.1757G>C
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|
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ENST00000679928.1:c.*2038G>C
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ENSP00000506071.1:n.*2038G>C
|
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ENST00000680528.1:n.2452G>C
|
|
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ENST00000680999.1:c.1699G>C
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ENSP00000504984.1:p.Gly567Arg
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ENST00000681282.1:c.*1673G>C
|
ENSP00000506339.1:n.*1673G>C
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|
ENST00000333213.10:c.1486G>C
|
ENSP00000327487.6:p.Gly496Arg
|
|
ENST00000545228.2:c.763G>C
|
|
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ENST00000577197.1:n.234G>C
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|
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ENST00000579449.1:n.683G>C
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|
|
NM_207346.2:c.1486G>C
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NP_997229.2:p.Gly496Arg
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XM_005257229.2:c.1674G>C
|
XP_005257286.1:p.Val558=
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XM_006721821.2:c.1371G>C
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XP_006721884.1:p.Val457=
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XM_011524616.1:c.1557G>C
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XP_011522918.1:p.Val519=
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XM_011524617.1:c.*68G>C
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XP_011522919.1:n.*68G>C
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XM_011524618.1:c.1369G>C
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XP_011522920.1:p.Gly457Arg
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XR_243646.2:n.1718G>C
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|
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XM_005257229.4:c.1674G>C
|
XP_005257286.1:p.Val558=
|
|
XR_001753015.1:n.81C>G
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|
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XR_001753016.1:n.82C>G
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XR_243646.4:n.1724G>C
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NM_207346.3:c.1486G>C
MANE Select
|
NP_997229.2:p.Gly496Arg
|
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