ENST00000286657.10:c.1682G=
MANE Select
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ENSP00000286657.4:p.Gly561=
|
|
ENST00000286657.8:c.1682G=
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ENSP00000286657.4:p.Gly561=
|
|
ENST00000622135.1:c.1682G=
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ENSP00000480055.1:p.Gly561=
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|
NM_014243.2:c.1682G=
|
NP_055058.2:p.Gly561=
|
|
XM_011532421.1:c.1625G=
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XP_011530723.1:p.Gly542=
|
|
XM_011532422.1:c.1598G=
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XP_011530724.1:p.Gly533=
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XM_011532423.1:c.1040G=
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XP_011530725.1:p.Gly347=
|
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XM_011532424.1:c.950G=
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XP_011530726.1:p.Gly317=
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XM_011532421.2:c.1625G=
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XP_011530723.1:p.Gly542=
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|
XM_011532422.3:c.1598G=
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XP_011530724.1:p.Gly533=
|
|
NM_014243.3:c.1682G=
MANE Select
|
NP_055058.2:p.Gly561=
|
|