ENST00000295897.9:c.1803T>G
MANE Select
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ENSP00000295897.4:p.Ala601=
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ENST00000295897.8:c.1803T>G
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ENSP00000295897.4:p.Ala601=
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ENST00000401494.7:c.1458T>G
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ENSP00000384695.3:p.Ala486=
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ENST00000415165.6:c.1227T>G
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ENSP00000401820.2:p.Ala409=
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ENST00000476441.6:c.*1082T>G
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ENSP00000423727.1:n.*1082T>G
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ENST00000495173.1:n.111T>G
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|
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ENST00000503124.5:c.1353T>G
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ENSP00000421027.1:p.Ala451=
|
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ENST00000505649.5:n.1350T>G
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|
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ENST00000508932.5:n.193T>G
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|
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ENST00000509063.5:c.1785+632T>G
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ENSP00000422784.1:n.1785+632T>G
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ENST00000511370.1:c.1336T>G
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|
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ENST00000621085.4:c.1164T>G
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ENSP00000483421.1:p.Ala388=
|
|
ENST00000621628.4:c.1164T>G
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ENSP00000480485.1:p.Ala388=
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NM_000477.5:c.1803T>G
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NP_000468.1:p.Ala601=
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NM_000477.6:c.1803T>G
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NP_000468.1:p.Ala601=
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NM_000477.7:c.1803T>G
MANE Select
|
NP_000468.1:p.Ala601=
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