ENST00000695666.1:n.958T>G
|
|
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ENST00000695667.1:n.476T>G
|
|
|
ENST00000300692.9:c.406+65T>G
MANE Select
|
ENSP00000300692.4:n.406+65T>G
|
|
ENST00000300692.8:c.406+65T>G
|
ENSP00000300692.4:n.406+65T>G
|
|
ENST00000392884.2:c.275-216T>G
|
ENSP00000376622.2:n.275-216T>G
|
|
ENST00000526561.1:n.80-216T>G
|
|
|
ENST00000529594.5:c.187+65T>G
|
ENSP00000437335.1:n.187+65T>G
|
|
ENST00000534687.5:c.288-216T>G
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|
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NM_000732.4:c.406+65T>G , LRG_37t1:c.406+65T>G
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NP_000723.1:n.406+65T>G
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NM_001040651.1:c.275-216T>G
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NP_001035741.1:n.275-216T>G
|
|
NM_001040651.2:c.275-216T>G
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NP_001035741.1:n.275-216T>G
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|
NM_000732.6:c.406+65T>G
MANE Select
|
NP_000723.1:n.406+65T>G
|
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