ENST00000695850.1:n.1678A>G
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ENST00000695852.1:n.609A>G
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ENST00000695853.1:c.*1561A>G
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ENSP00000512218.1:n.*1561A>G
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ENST00000423902.7:c.8502A>G
MANE Select
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ENSP00000392028.1:p.Gly2834=
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ENST00000423902.6:c.8502A>G
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ENSP00000392028.1:p.Gly2834=
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ENST00000524602.5:c.2355A>G
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ENSP00000437061.1:p.Gly785=
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ENST00000528280.1:n.548A>G
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NM_001316690.1:c.2355A>G
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NP_001303619.1:p.Gly785=
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NM_017780.3:c.8502A>G
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NP_060250.2:p.Gly2834=
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XM_011517553.1:c.8592A>G
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XP_011515855.1:p.Gly2864=
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XM_011517554.1:c.8592A>G
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XP_011515856.1:p.Gly2864=
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XM_011517555.1:c.8589A>G
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XP_011515857.1:p.Gly2863=
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XM_011517556.1:c.8370A>G
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XP_011515858.1:p.Gly2790=
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XM_011517557.1:c.6579A>G
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XP_011515859.1:p.Gly2193=
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XM_011517558.1:c.6129A>G
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XP_011515860.1:p.Gly2043=
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XM_011517559.1:c.5337A>G
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XP_011515861.1:p.Gly1779=
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XM_011517553.2:c.8592A>G
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XP_011515855.1:p.Gly2864=
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XM_011517554.3:c.8592A>G
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XP_011515856.1:p.Gly2864=
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XM_011517555.2:c.8589A>G
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XP_011515857.1:p.Gly2863=
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XM_017013612.1:c.8592A>G
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XP_016869101.1:p.Gly2864=
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XM_017013613.1:c.8499A>G
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XP_016869102.1:p.Gly2833=
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NM_017780.4:c.8502A>G
MANE Select
|
NP_060250.2:p.Gly2834=
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