ENST00000497571.6:c.532G>T
MANE Select
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ENSP00000419923.1:p.Gly178Trp
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ENST00000173785.4:n.257+10G>T
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ENST00000469435.1:c.532G>T
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ENSP00000419079.1:p.Gly178Trp
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ENST00000497571.5:c.532G>T
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ENSP00000419923.1:p.Gly178Trp
|
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ENST00000542957.1:c.532G>T
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ENSP00000445301.1:p.Gly178Trp
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NM_001160124.1:c.532G>T
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NP_001153596.1:p.Gly178Trp
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NM_001160125.1:c.532G>T
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NP_001153597.1:p.Gly178Trp
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NM_001300.5:c.532G>T
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NP_001291.3:p.Gly178Trp
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NR_027653.1:n.789+10G>T
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NM_001300.6:c.532G>T
MANE Select
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NP_001291.3:p.Gly178Trp
|
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NM_001160124.2:c.532G>T
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NP_001153596.1:p.Gly178Trp
|
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NR_027653.2:n.717+10G>T
|
|
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NM_001160125.2:c.532G>T
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NP_001153597.1:p.Gly178Trp
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