ENST00000649046.1:c.12205C=
MANE Select
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ENSP00000496870.1:p.Leu4069=
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ENST00000649153.1:c.3105C=
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|
|
ENST00000650252.1:c.1233C=
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ENSP00000496887.1:p.Ile411=
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ENST00000263816.7:c.12205C=
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ENSP00000263816.3:p.Leu4069=
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|
NM_004525.2:c.12205C=
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NP_004516.2:p.Leu4069=
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|
XM_011511183.1:c.12076C=
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XP_011509485.1:p.Leu4026=
|
|
XM_011511184.1:c.9916C=
|
XP_011509486.1:p.Leu3306=
|
|
NM_004525.3:c.12205C=
MANE Select
|
NP_004516.2:p.Leu4069=
|
|
XM_011511183.3:c.12076C=
|
XP_011509485.1:p.Leu4026=
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|
XM_011511184.2:c.9916C=
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XP_011509486.1:p.Leu3306=
|
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