ENST00000225964.10:c.1767+325C>A
MANE Select
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ENSP00000225964.6:n.1767+325C>A
|
|
ENST00000225964.9:c.1767+325C>A
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ENSP00000225964.5:n.1767+325C>A
|
|
ENST00000463440.1:n.482C>A
|
|
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ENST00000471344.1:n.1124C>A
|
|
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ENST00000476387.1:n.116+325C>A
|
|
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NM_000088.3:c.1767+325C>A , LRG_1t1:c.1767+325C>A
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NP_000079.2:n.1767+325C>A
|
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XM_005257058.3:c.1767+325C>A
|
XP_005257115.2:n.1767+325C>A
|
|
XM_005257059.3:c.958-925C>A
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XP_005257116.2:n.958-925C>A
|
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XM_011524341.1:c.1569+325C>A
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XP_011522643.1:n.1569+325C>A
|
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XM_005257058.4:c.1767+325C>A
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XP_005257115.2:n.1767+325C>A
|
|
XM_005257059.4:c.958-925C>A
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XP_005257116.2:n.958-925C>A
|
|
NM_000088.4:c.1767+325C>A
MANE Select
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NP_000079.2:n.1767+325C>A
|
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