ENST00000295897.9:c.1788T>C
MANE Select
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ENSP00000295897.4:p.Gly596=
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ENST00000295897.8:c.1788T>C
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ENSP00000295897.4:p.Gly596=
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ENST00000401494.7:c.1443T>C
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ENSP00000384695.3:p.Gly481=
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ENST00000415165.6:c.1212T>C
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ENSP00000401820.2:p.Gly404=
|
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ENST00000476441.6:c.*1067T>C
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ENSP00000423727.1:n.*1067T>C
|
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ENST00000495173.1:n.96T>C
|
|
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ENST00000503124.5:c.1338T>C
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ENSP00000421027.1:p.Gly446=
|
|
ENST00000505649.5:n.1335T>C
|
|
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ENST00000508932.5:n.178T>C
|
|
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ENST00000509063.5:c.1785+617T>C
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ENSP00000422784.1:n.1785+617T>C
|
|
ENST00000511370.1:c.1321T>C
|
|
|
ENST00000621085.4:c.1149T>C
|
ENSP00000483421.1:p.Gly383=
|
|
ENST00000621628.4:c.1149T>C
|
ENSP00000480485.1:p.Gly383=
|
|
NM_000477.5:c.1788T>C
|
NP_000468.1:p.Gly596=
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|
NM_000477.6:c.1788T>C
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NP_000468.1:p.Gly596=
|
|
NM_000477.7:c.1788T>C
MANE Select
|
NP_000468.1:p.Gly596=
|
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