ENST00000295897.9:c.1802C=
MANE Select
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ENSP00000295897.4:p.Ala601=
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ENST00000295897.8:c.1802C=
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ENSP00000295897.4:p.Ala601=
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|
ENST00000401494.7:c.1457C=
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ENSP00000384695.3:p.Ala486=
|
|
ENST00000415165.6:c.1226C=
|
ENSP00000401820.2:p.Ala409=
|
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ENST00000476441.6:c.*1081C=
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ENSP00000423727.1:n.*1081C=
|
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ENST00000495173.1:n.110C=
|
|
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ENST00000503124.5:c.1352C=
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ENSP00000421027.1:p.Ala451=
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|
ENST00000505649.5:n.1349C=
|
|
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ENST00000508932.5:n.192C=
|
|
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ENST00000509063.5:c.1785+631C=
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ENSP00000422784.1:n.1785+631C=
|
|
ENST00000511370.1:c.1335C=
|
|
|
ENST00000621085.4:c.1163C=
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ENSP00000483421.1:p.Ala388=
|
|
ENST00000621628.4:c.1163C=
|
ENSP00000480485.1:p.Ala388=
|
|
NM_000477.5:c.1802C=
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NP_000468.1:p.Ala601=
|
|
NM_000477.6:c.1802C=
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NP_000468.1:p.Ala601=
|
|
NM_000477.7:c.1802C=
MANE Select
|
NP_000468.1:p.Ala601=
|
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