ENST00000392666.6:c.625G>T
MANE Select
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ENSP00000376434.1:p.Gly209Ter
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ENST00000324036.7:c.625G>T
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ENSP00000316233.3:p.Gly209Ter
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ENST00000392664.2:c.682G>T
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ENSP00000376432.2:p.Gly228Ter
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ENST00000392665.6:c.625G>T
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ENSP00000376433.2:p.Gly209Ter
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ENST00000392666.5:c.625G>T
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ENSP00000376434.1:p.Gly209Ter
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ENST00000440599.6:c.625G>T
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ENSP00000406320.2:p.Gly209Ter
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NM_000220.4:c.682G>T
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NP_000211.1:p.Gly228Ter
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NM_153764.2:c.625G>T
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NP_722448.1:p.Gly209Ter
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NM_153765.2:c.676G>T
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NP_722449.3:p.Gly226Ter
|
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NM_153766.2:c.625G>T
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NP_722450.1:p.Gly209Ter
|
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NM_153767.3:c.625G>T
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NP_722451.1:p.Gly209Ter
|
|
NM_000220.6:c.682G>T
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NP_000211.1:p.Gly228Ter
|
|
NM_153764.3:c.625G>T
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NP_722448.1:p.Gly209Ter
|
|
NM_153765.3:c.676G>T
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NP_722449.3:p.Gly226Ter
|
|
NM_153766.3:c.625G>T
MANE Select
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NP_722450.1:p.Gly209Ter
|
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NM_153767.4:c.625G>T
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NP_722451.1:p.Gly209Ter
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