ENST00000281928.9:c.5175+96G>C
MANE Select
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ENSP00000281928.3:n.5175+96G>C
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ENST00000549786.2:c.4699G>C
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|
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ENST00000648379.1:n.3543+96G>C
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|
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ENST00000648737.1:n.4939+96G>C
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ENST00000648825.1:n.2011G>C
|
|
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ENST00000648916.1:n.3186+96G>C
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|
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ENST00000649146.1:n.2514G>C
|
|
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ENST00000649607.1:c.3359+96G>C
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|
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ENST00000649775.1:c.1664+96G>C
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|
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ENST00000650226.1:c.5175+96G>C
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ENSP00000496981.1:n.5175+96G>C
|
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ENST00000281928.7:c.5175+96G>C
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ENSP00000281928.3:n.5175+96G>C
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ENST00000549786.1:c.635G>C
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|
|
ENST00000552340.1:c.207+96G>C
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ENSP00000449876.1:n.207+96G>C
|
|
NM_015335.4:c.5175+96G>C
|
NP_056150.1:n.5175+96G>C
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|
XM_011538080.1:c.5175+96G>C
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XP_011536382.1:n.5175+96G>C
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XM_011538081.1:c.5172+96G>C
|
XP_011536383.1:n.5172+96G>C
|
|
XM_011538082.1:c.5145+96G>C
|
XP_011536384.1:n.5145+96G>C
|
|
XM_011538080.2:c.5175+96G>C
|
XP_011536382.1:n.5175+96G>C
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|
XM_011538081.2:c.5172+96G>C
|
XP_011536383.1:n.5172+96G>C
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XM_011538082.2:c.5145+96G>C
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XP_011536384.1:n.5145+96G>C
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|
XM_017019090.1:c.5172+96G>C
|
XP_016874579.1:n.5172+96G>C
|
|
NM_015335.5:c.5175+96G>C
MANE Select
|
NP_056150.1:n.5175+96G>C
|
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