ENST00000260210.5:c.1775G>C
MANE Select
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ENSP00000260210.3:p.Gly592Ala
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ENST00000260210.4:c.1775G>C
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ENSP00000260210.3:p.Gly592Ala
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ENST00000375445.7:c.1373G>C
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ENSP00000364594.3:p.Gly458Ala
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ENST00000419189.1:c.550G>C
|
|
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NM_001159736.1:c.1373G>C
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NP_001153208.1:p.Gly458Ala
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NM_032725.3:c.1775G>C
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NP_116114.1:p.Gly592Ala
|
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XM_011543035.1:c.1676G>C
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XP_011541337.1:p.Gly559Ala
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XM_011543035.2:c.1676G>C
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XP_011541337.1:p.Gly559Ala
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NM_032725.4:c.1775G>C
MANE Select
|
NP_116114.1:p.Gly592Ala
|
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NM_001159736.2:c.1373G>C
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NP_001153208.1:p.Gly458Ala
|
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