ENST00000348931.9:c.593G>C
MANE Select
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ENSP00000335384.5:p.Gly198Ala
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ENST00000348931.8:c.593G>C
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ENSP00000335384.5:p.Gly198Ala
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ENST00000377940.3:c.527G>C
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ENSP00000367174.3:p.Gly176Ala
|
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ENST00000583811.5:c.239G>C
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ENSP00000462463.1:p.Gly80Ala
|
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ENST00000584588.5:c.407-588G>C
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ENSP00000462067.1:n.407-588G>C
|
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NM_198844.2:c.527G>C
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NP_942141.2:p.Gly176Ala
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NM_199321.2:c.593G>C
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NP_955353.1:p.Gly198Ala
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XM_011524298.1:c.593G>C
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XP_011522600.1:p.Gly198Ala
|
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XR_002957959.1:n.784G>C
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|
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NM_198844.3:c.527G>C
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NP_942141.2:p.Gly176Ala
|
|
NM_199321.3:c.593G>C
MANE Select
|
NP_955353.1:p.Gly198Ala
|
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