ENST00000695666.1:n.1020A=
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|
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ENST00000695667.1:n.538A=
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|
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ENST00000300692.9:c.406+127A=
MANE Select
|
ENSP00000300692.4:n.406+127A=
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|
ENST00000300692.8:c.406+127A=
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ENSP00000300692.4:n.406+127A=
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|
ENST00000392884.2:c.275-154A=
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ENSP00000376622.2:n.275-154A=
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ENST00000526561.1:n.80-154A=
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|
|
ENST00000529594.5:c.187+127A=
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ENSP00000437335.1:n.187+127A=
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|
ENST00000534687.5:c.288-154A=
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|
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NM_000732.4:c.406+127A= , LRG_37t1:c.406+127A=
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NP_000723.1:n.406+127A=
|
|
NM_001040651.1:c.275-154A=
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NP_001035741.1:n.275-154A=
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|
NM_001040651.2:c.275-154A=
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NP_001035741.1:n.275-154A=
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|
NM_000732.6:c.406+127A=
MANE Select
|
NP_000723.1:n.406+127A=
|
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