ENST00000375128.5:c.674-183G>T
MANE Select
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ENSP00000364270.5:n.674-183G>T
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ENST00000375128.4:c.674-183G>T
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ENSP00000364270.4:n.674-183G>T
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ENST00000462523.5:c.*110-183G>T
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ENSP00000433006.1:n.*110-183G>T
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ENST00000485042.1:n.185+1G>T
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NM_000380.3:c.674-183G>T , LRG_471t1:c.674-183G>T
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NP_000371.1:n.674-183G>T
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NR_027302.1:n.1022-183G>T
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|
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XM_006717278.1:c.674-183G>T
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XP_006717341.1:n.674-183G>T
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XM_011518988.1:c.674-183G>T
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XP_011517290.1:n.674-183G>T
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XR_929839.1:n.1204+1G>T
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|
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NM_001354975.1:c.548-183G>T
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NP_001341904.1:n.548-183G>T
|
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NR_149091.1:n.519-183G>T
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|
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NR_149092.1:n.685-183G>T
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|
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NR_149093.1:n.1210+1G>T
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|
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NR_149094.1:n.1104+1G>T
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|
|
NM_000380.4:c.674-183G>T
MANE Select
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NP_000371.1:n.674-183G>T
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NM_001354975.2:c.548-183G>T
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NP_001341904.1:n.548-183G>T
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NR_027302.2:n.953-183G>T
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|
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NR_149091.2:n.450-183G>T
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|
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NR_149092.2:n.616-183G>T
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|
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NR_149093.2:n.1141+1G>T
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|
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NR_149094.2:n.1035+1G>T
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