ENST00000375128.5:c.724C>G
MANE Select
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ENSP00000364270.5:p.His242Asp
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ENST00000375128.4:c.724C>G
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ENSP00000364270.4:p.His242Asp
|
|
ENST00000462523.5:c.*160C>G
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ENSP00000433006.1:n.*160C>G
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ENST00000485042.1:n.236C>G
|
|
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NM_000380.3:c.724C>G , LRG_471t1:c.724C>G
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NP_000371.1:p.His242Asp
|
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NR_027302.1:n.1072C>G
|
|
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XM_006717278.1:c.724C>G
|
XP_006717341.1:p.His242Asp
|
|
XM_011518988.1:c.724C>G
|
XP_011517290.1:p.His242Asp
|
|
XR_929839.1:n.1255C>G
|
|
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NM_001354975.1:c.598C>G
|
NP_001341904.1:p.His200Asp
|
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NR_149091.1:n.569C>G
|
|
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NR_149092.1:n.735C>G
|
|
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NR_149093.1:n.1261C>G
|
|
|
NR_149094.1:n.1155C>G
|
|
|
NM_000380.4:c.724C>G
MANE Select
|
NP_000371.1:p.His242Asp
|
|
NM_001354975.2:c.598C>G
|
NP_001341904.1:p.His200Asp
|
|
NR_027302.2:n.1003C>G
|
|
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NR_149091.2:n.500C>G
|
|
|
NR_149092.2:n.666C>G
|
|
|
NR_149093.2:n.1192C>G
|
|
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NR_149094.2:n.1086C>G
|
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