ENST00000400521.7:c.1089G>C
MANE Select
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ENSP00000383365.1:p.Gly363=
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ENST00000400518.5:c.999G>C
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ENSP00000383362.1:p.Gly333=
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ENST00000400519.6:c.1086G>C
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ENSP00000383363.1:p.Gly362=
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ENST00000400521.6:c.1089G>C
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ENSP00000383365.1:p.Gly363=
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ENST00000400525.6:c.1020G>C
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ENSP00000383369.3:p.Gly340=
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ENST00000462330.5:c.12G>C
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ENSP00000485603.2:p.Gly4=
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ENST00000462843.2:c.39G>C
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ENSP00000485466.2:p.Gly13=
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ENST00000474308.5:c.1032G>C
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ENSP00000485665.1:p.Gly344=
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ENST00000485358.5:c.57G>C
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ENSP00000485499.2:p.Gly19=
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ENST00000487165.5:n.1183G>C
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ENST00000494454.5:n.1163G>C
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ENST00000495655.2:n.633G>C
|
|
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ENST00000542719.6:c.801G>C
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ENSP00000485128.2:p.Gly267=
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ENST00000634471.1:n.244-444G>C
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ENST00000634537.1:c.318G>C
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ENSP00000489208.1:p.Gly106=
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NM_006440.4:c.1089G>C
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NP_006431.2:p.Gly363=
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NM_001352300.1:c.1086G>C
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NP_001339229.1:p.Gly362=
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NM_001352301.1:c.999G>C
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NP_001339230.1:p.Gly333=
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NM_001352302.1:c.801G>C
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NP_001339231.1:p.Gly267=
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NR_147957.1:n.1221G>C
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|
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NM_006440.5:c.1089G>C
MANE Select
|
NP_006431.2:p.Gly363=
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NM_001352300.2:c.1086G>C
|
NP_001339229.1:p.Gly362=
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NR_147957.2:n.1047G>C
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|
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NM_001352301.2:c.999G>C
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NP_001339230.1:p.Gly333=
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NM_001352302.2:c.801G>C
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NP_001339231.1:p.Gly267=
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