ENST00000375128.5:c.730C>G
MANE Select
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ENSP00000364270.5:p.His244Asp
|
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ENST00000375128.4:c.730C>G
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ENSP00000364270.4:p.His244Asp
|
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ENST00000462523.5:c.*166C>G
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ENSP00000433006.1:n.*166C>G
|
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ENST00000485042.1:n.242C>G
|
|
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NM_000380.3:c.730C>G , LRG_471t1:c.730C>G
|
NP_000371.1:p.His244Asp
|
|
NR_027302.1:n.1078C>G
|
|
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XM_006717278.1:c.730C>G
|
XP_006717341.1:p.His244Asp
|
|
XM_011518988.1:c.730C>G
|
XP_011517290.1:p.His244Asp
|
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XR_929839.1:n.1261C>G
|
|
|
NM_001354975.1:c.604C>G
|
NP_001341904.1:p.His202Asp
|
|
NR_149091.1:n.575C>G
|
|
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NR_149092.1:n.741C>G
|
|
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NR_149093.1:n.1267C>G
|
|
|
NR_149094.1:n.1161C>G
|
|
|
NM_000380.4:c.730C>G
MANE Select
|
NP_000371.1:p.His244Asp
|
|
NM_001354975.2:c.604C>G
|
NP_001341904.1:p.His202Asp
|
|
NR_027302.2:n.1009C>G
|
|
|
NR_149091.2:n.506C>G
|
|
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NR_149092.2:n.672C>G
|
|
|
NR_149093.2:n.1198C>G
|
|
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NR_149094.2:n.1092C>G
|
|
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