ENST00000225964.10:c.4248+11A>G
MANE Select
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ENSP00000225964.6:n.4248+11A>G
|
|
ENST00000225964.9:c.4248+11A>G
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ENSP00000225964.5:n.4248+11A>G
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NM_000088.3:c.4248+11A>G , LRG_1t1:c.4248+11A>G
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NP_000079.2:n.4248+11A>G
|
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XM_005257058.3:c.3978+11A>G
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XP_005257115.2:n.3978+11A>G
|
|
XM_005257059.3:c.3330+11A>G
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XP_005257116.2:n.3330+11A>G
|
|
XM_011524341.1:c.4050+11A>G
|
XP_011522643.1:n.4050+11A>G
|
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XM_005257058.4:c.3978+11A>G
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XP_005257115.2:n.3978+11A>G
|
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XM_005257059.4:c.3330+11A>G
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XP_005257116.2:n.3330+11A>G
|
|
NM_000088.4:c.4248+11A>G
MANE Select
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NP_000079.2:n.4248+11A>G
|
|