ENST00000352480.10:c.1040G>C
MANE Select
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ENSP00000253004.6:p.Gly347Ala
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ENST00000352480.9:c.1040G>C
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ENSP00000253004.6:p.Gly347Ala
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ENST00000372386.6:n.311G>C
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ENST00000372393.7:c.1040G>C
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ENSP00000361469.2:p.Gly347Ala
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ENST00000372394.5:c.1040G>C
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ENSP00000361471.1:p.Gly347Ala
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NM_000050.4:c.1040G>C
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NP_000041.2:p.Gly347Ala
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NM_054012.3:c.1040G>C
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NP_446464.1:p.Gly347Ala
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XM_005272200.2:c.1040G>C
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XP_005272257.1:p.Gly347Ala
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XM_011518705.1:c.1154G>C
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XP_011517007.1:p.Gly385Ala
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XR_930393.1:n.1060-2679C>G
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XM_005272200.3:c.1040G>C
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XP_005272257.1:p.Gly347Ala
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XM_011518705.2:c.1154G>C
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XP_011517007.1:p.Gly385Ala
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XM_017014729.1:c.1136G>C
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XP_016870218.1:p.Gly379Ala
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XR_930393.2:n.1102-2679C>G
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NM_054012.4:c.1040G>C
MANE Select
|
NP_446464.1:p.Gly347Ala
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