ENST00000367435.5:c.693G=
MANE Select
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ENSP00000356405.4:p.Trp231=
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|
ENST00000635846.1:c.693G=
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ENSP00000490035.1:p.Trp231=
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|
ENST00000643006.1:c.693G=
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ENSP00000496633.1:p.Trp231=
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ENST00000643784.1:c.*169G=
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ENSP00000494944.1:n.*169G=
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ENST00000647662.1:n.594G=
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|
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ENST00000648071.1:c.*669G=
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ENSP00000497513.1:n.*669G=
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|
ENST00000649606.1:n.706G=
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|
|
ENST00000649895.1:n.911G=
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|
|
ENST00000650197.1:c.693G=
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ENSP00000496929.1:p.Trp231=
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|
ENST00000367435.3:c.693G=
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ENSP00000356405.3:p.Trp231=
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|
NM_024529.4:c.693G= , LRG_507t1:c.693G=
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NP_078805.3:p.Trp231=
|
|
XM_006711537.2:c.693G=
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XP_006711600.1:p.Trp231=
|
|
XM_006711537.4:c.693G=
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XP_006711600.1:p.Trp231=
|
|
NM_024529.5:c.693G=
MANE Select
|
NP_078805.3:p.Trp231=
|
|