ENST00000599672.6:c.231A>G
MANE Select
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ENSP00000470560.1:p.Gly77=
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ENST00000261406.7:c.213A>G
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ENSP00000476966.2:p.Gly71=
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ENST00000539196.2:c.94A>G
|
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ENST00000599672.5:c.231A>G
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ENSP00000470560.1:p.Gly77=
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ENST00000607161.5:c.234A>G
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ENSP00000480420.1:p.Gly78=
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ENST00000611981.1:n.242A>G
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ENST00000620255.1:n.220A>G
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NM_006331.7:c.231A>G
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NP_006322.4:p.Gly77=
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XM_011520907.1:c.231A>G
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XP_011519209.1:p.Gly77=
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NM_001320049.1:c.231A>G
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NP_001306978.1:p.Gly77=
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NR_135131.1:n.374A>G
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NM_006331.8:c.231A>G
MANE Select
|
NP_006322.4:p.Gly77=
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NM_001320049.2:c.231A>G
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NP_001306978.1:p.Gly77=
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NR_135131.2:n.242A>G
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