ENST00000375128.5:c.767T>G
MANE Select
|
ENSP00000364270.5:p.Met256Arg
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ENST00000375128.4:c.767T>G
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ENSP00000364270.4:p.Met256Arg
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ENST00000462523.5:c.*203T>G
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ENSP00000433006.1:n.*203T>G
|
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ENST00000485042.1:n.279T>G
|
|
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NM_000380.3:c.767T>G , LRG_471t1:c.767T>G
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NP_000371.1:p.Met256Arg
|
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NR_027302.1:n.1115T>G
|
|
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XM_006717278.1:c.767T>G
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XP_006717341.1:p.Met256Arg
|
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XM_011518988.1:c.767T>G
|
XP_011517290.1:p.Met256Arg
|
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NM_001354975.1:c.641T>G
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NP_001341904.1:p.Met214Arg
|
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NR_149091.1:n.612T>G
|
|
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NR_149092.1:n.778T>G
|
|
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NR_149093.1:n.1304T>G
|
|
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NR_149094.1:n.1198T>G
|
|
|
NM_000380.4:c.767T>G
MANE Select
|
NP_000371.1:p.Met256Arg
|
|
NM_001354975.2:c.641T>G
|
NP_001341904.1:p.Met214Arg
|
|
NR_027302.2:n.1046T>G
|
|
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NR_149091.2:n.543T>G
|
|
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NR_149092.2:n.709T>G
|
|
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NR_149093.2:n.1235T>G
|
|
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NR_149094.2:n.1129T>G
|
|
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