ENST00000262887.10:c.618A>C
MANE Select
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ENSP00000262887.5:p.Pro206=
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ENST00000262887.9:c.618A>C
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ENSP00000262887.4:p.Pro206=
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ENST00000543982.5:c.525A>C
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ENSP00000443671.1:p.Pro175=
|
|
ENST00000594107.1:c.507A>C
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ENSP00000471159.1:p.Pro169=
|
|
ENST00000595789.5:n.666A>C
|
|
|
ENST00000597811.5:c.387-232A>C
|
|
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ENST00000598165.5:c.639A>C
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ENSP00000470045.1:p.Pro213=
|
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ENST00000598422.1:n.298A>C
|
|
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ENST00000599693.5:c.544A>C
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|
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NM_006297.2:c.618A>C , LRG_784t1:c.618A>C
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NP_006288.2:p.Pro206=
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NM_006297.3:c.618A>C
MANE Select
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NP_006288.2:p.Pro206=
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|