ENST00000225964.10:c.3207+18A>G
MANE Select
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ENSP00000225964.6:n.3207+18A>G
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ENST00000225964.9:c.3207+18A>G
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ENSP00000225964.5:n.3207+18A>G
|
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ENST00000486572.1:n.43A>G
|
|
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ENST00000511732.1:n.169A>G
|
|
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NM_000088.3:c.3207+18A>G , LRG_1t1:c.3207+18A>G
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NP_000079.2:n.3207+18A>G
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XM_005257058.3:c.2937+18A>G
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XP_005257115.2:n.2937+18A>G
|
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XM_005257059.3:c.2289+18A>G
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XP_005257116.2:n.2289+18A>G
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XM_011524341.1:c.3009+18A>G
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XP_011522643.1:n.3009+18A>G
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XM_005257058.4:c.2937+18A>G
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XP_005257115.2:n.2937+18A>G
|
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XM_005257059.4:c.2289+18A>G
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XP_005257116.2:n.2289+18A>G
|
|
NM_000088.4:c.3207+18A>G
MANE Select
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NP_000079.2:n.3207+18A>G
|
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