ENST00000375128.5:c.722T>G
MANE Select
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ENSP00000364270.5:p.Val241Gly
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ENST00000375128.4:c.722T>G
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ENSP00000364270.4:p.Val241Gly
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ENST00000462523.5:c.*158T>G
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ENSP00000433006.1:n.*158T>G
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ENST00000485042.1:n.234T>G
|
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NM_000380.3:c.722T>G , LRG_471t1:c.722T>G
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NP_000371.1:p.Val241Gly
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NR_027302.1:n.1070T>G
|
|
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XM_006717278.1:c.722T>G
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XP_006717341.1:p.Val241Gly
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XM_011518988.1:c.722T>G
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XP_011517290.1:p.Val241Gly
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XR_929839.1:n.1253T>G
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NM_001354975.1:c.596T>G
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NP_001341904.1:p.Val199Gly
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NR_149091.1:n.567T>G
|
|
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NR_149092.1:n.733T>G
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NR_149093.1:n.1259T>G
|
|
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NR_149094.1:n.1153T>G
|
|
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NM_000380.4:c.722T>G
MANE Select
|
NP_000371.1:p.Val241Gly
|
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NM_001354975.2:c.596T>G
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NP_001341904.1:p.Val199Gly
|
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NR_027302.2:n.1001T>G
|
|
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NR_149091.2:n.498T>G
|
|
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NR_149092.2:n.664T>G
|
|
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NR_149093.2:n.1190T>G
|
|
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NR_149094.2:n.1084T>G
|
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