ENST00000225964.10:c.3207+77G>A
MANE Select
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ENSP00000225964.6:n.3207+77G>A
|
|
ENST00000225964.9:c.3207+77G>A
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ENSP00000225964.5:n.3207+77G>A
|
|
ENST00000486572.1:n.102G>A
|
|
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ENST00000511732.1:n.228G>A
|
|
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NM_000088.3:c.3207+77G>A , LRG_1t1:c.3207+77G>A
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NP_000079.2:n.3207+77G>A
|
|
XM_005257058.3:c.2937+77G>A
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XP_005257115.2:n.2937+77G>A
|
|
XM_005257059.3:c.2289+77G>A
|
XP_005257116.2:n.2289+77G>A
|
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XM_011524341.1:c.3009+77G>A
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XP_011522643.1:n.3009+77G>A
|
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XM_005257058.4:c.2937+77G>A
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XP_005257115.2:n.2937+77G>A
|
|
XM_005257059.4:c.2289+77G>A
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XP_005257116.2:n.2289+77G>A
|
|
NM_000088.4:c.3207+77G>A
MANE Select
|
NP_000079.2:n.3207+77G>A
|
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