ENST00000367435.5:c.639T>C
MANE Select
|
ENSP00000356405.4:p.Phe213=
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|
ENST00000635846.1:c.639T>C
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ENSP00000490035.1:p.Phe213=
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|
ENST00000643006.1:c.639T>C
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ENSP00000496633.1:p.Phe213=
|
|
ENST00000643784.1:c.*115T>C
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ENSP00000494944.1:n.*115T>C
|
|
ENST00000647662.1:n.540T>C
|
|
|
ENST00000648071.1:c.*615T>C
|
ENSP00000497513.1:n.*615T>C
|
|
ENST00000649606.1:n.652T>C
|
|
|
ENST00000649895.1:n.857T>C
|
|
|
ENST00000650197.1:c.639T>C
|
ENSP00000496929.1:p.Phe213=
|
|
ENST00000367435.3:c.639T>C
|
ENSP00000356405.3:p.Phe213=
|
|
NM_024529.4:c.639T>C , LRG_507t1:c.639T>C
|
NP_078805.3:p.Phe213=
|
|
XM_006711537.2:c.639T>C
|
XP_006711600.1:p.Phe213=
|
|
XM_006711537.4:c.639T>C
|
XP_006711600.1:p.Phe213=
|
|
NM_024529.5:c.639T>C
MANE Select
|
NP_078805.3:p.Phe213=
|
|