ENST00000649046.1:c.13753C=
MANE Select
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ENSP00000496870.1:p.Arg4585=
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ENST00000649153.1:c.4562C=
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|
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ENST00000650252.1:c.2744C=
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ENSP00000496887.1:n.2744C=
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ENST00000263816.7:c.13753C=
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ENSP00000263816.3:p.Arg4585=
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NM_004525.2:c.13753C=
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NP_004516.2:p.Arg4585=
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XM_011511183.1:c.13624C=
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XP_011509485.1:p.Arg4542=
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|
XM_011511184.1:c.11464C=
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XP_011509486.1:p.Arg3822=
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|
NM_004525.3:c.13753C=
MANE Select
|
NP_004516.2:p.Arg4585=
|
|
XM_011511183.3:c.13624C=
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XP_011509485.1:p.Arg4542=
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|
XM_011511184.2:c.11464C=
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XP_011509486.1:p.Arg3822=
|
|