ENST00000257904.11:c.479G>C
MANE Select
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ENSP00000257904.5:p.Gly160Ala
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ENST00000257904.10:c.479G>C
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ENSP00000257904.5:p.Gly160Ala
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ENST00000312990.10:c.265-295G>C
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ENSP00000316889.6:n.265-295G>C
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ENST00000546489.5:c.257G>C
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ENSP00000447779.1:p.Gly86Ala
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ENST00000547281.5:c.257G>C
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ENSP00000447274.1:p.Gly86Ala
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ENST00000549606.5:c.-158+1209G>C
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ENSP00000447005.1:n.-158+1209G>C
|
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ENST00000550419.5:c.479G>C
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ENSP00000448098.1:p.Gly160Ala
|
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ENST00000551706.1:n.845G>C
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|
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ENST00000551800.5:c.257G>C
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ENSP00000449391.1:p.Gly86Ala
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ENST00000551888.5:n.443-295G>C
|
|
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ENST00000552254.5:c.479G>C
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ENSP00000449179.1:p.Gly160Ala
|
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ENST00000552388.1:c.479G>C
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ENSP00000448963.1:p.Gly160Ala
|
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ENST00000553237.5:c.*118G>C
|
ENSP00000448885.1:n.*118G>C
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NM_000075.3:c.479G>C
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NP_000066.1:p.Gly160Ala
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NM_000075.4:c.479G>C
MANE Select
|
NP_000066.1:p.Gly160Ala
|
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