ENST00000295897.9:c.1822G>T
MANE Select
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ENSP00000295897.4:p.Gly608Cys
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ENST00000295897.8:c.1822G>T
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ENSP00000295897.4:p.Gly608Cys
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ENST00000401494.7:c.1477G>T
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ENSP00000384695.3:p.Gly493Cys
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ENST00000415165.6:c.1246G>T
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ENSP00000401820.2:p.Gly416Cys
|
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ENST00000476441.6:c.*1101G>T
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ENSP00000423727.1:n.*1101G>T
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ENST00000495173.1:n.130G>T
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|
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ENST00000503124.5:c.1372G>T
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ENSP00000421027.1:p.Gly458Cys
|
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ENST00000505649.5:n.1369G>T
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ENST00000508932.5:n.212G>T
|
|
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ENST00000509063.5:c.1785+651G>T
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ENSP00000422784.1:n.1785+651G>T
|
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ENST00000511370.1:c.1355G>T
|
|
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ENST00000621085.4:c.1183G>T
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ENSP00000483421.1:p.Gly395Cys
|
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ENST00000621628.4:c.1183G>T
|
ENSP00000480485.1:p.Gly395Cys
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NM_000477.5:c.1822G>T
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NP_000468.1:p.Gly608Cys
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NM_000477.6:c.1822G>T
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NP_000468.1:p.Gly608Cys
|
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NM_000477.7:c.1822G>T
MANE Select
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NP_000468.1:p.Gly608Cys
|
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