ENST00000373631.8:c.3695C>G
MANE Select
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ENSP00000362734.3:p.Ala1232Gly
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ENST00000373631.7:c.3695C>G
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ENSP00000362734.3:p.Ala1232Gly
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ENST00000460253.1:c.2699C>G
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ENSP00000435279.1:p.Ala900Gly
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NM_173689.6:c.3695C>G
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NP_775960.4:p.Ala1232Gly
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NR_104603.1:n.2809C>G
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XM_005251934.1:c.2699C>G
|
XP_005251991.1:p.Ala900Gly
|
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XM_011518556.1:c.3668C>G
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XP_011516858.1:p.Ala1223Gly
|
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XM_011518557.1:c.3500C>G
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XP_011516859.1:p.Ala1167Gly
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XM_011518558.1:c.3500C>G
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XP_011516860.1:p.Ala1167Gly
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XM_005251934.3:c.2699C>G
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XP_005251991.1:p.Ala900Gly
|
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XM_011518556.3:c.3668C>G
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XP_011516858.1:p.Ala1223Gly
|
|
XM_011518557.3:c.3500C>G
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XP_011516859.1:p.Ala1167Gly
|
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XM_011518558.3:c.3500C>G
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XP_011516860.1:p.Ala1167Gly
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|
NM_173689.7:c.3695C>G
MANE Select
|
NP_775960.4:p.Ala1232Gly
|
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NR_104603.2:n.2809C>G
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