ENST00000695850.1:n.1515C>G
|
|
|
ENST00000695852.1:n.446C>G
|
|
|
ENST00000695853.1:c.*1398C>G
|
ENSP00000512218.1:n.*1398C>G
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|
ENST00000423902.7:c.8339C>G
MANE Select
|
ENSP00000392028.1:p.Ala2780Gly
|
|
ENST00000423902.6:c.8339C>G
|
ENSP00000392028.1:p.Ala2780Gly
|
|
ENST00000524602.5:c.2192C>G
|
ENSP00000437061.1:p.Ala731Gly
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ENST00000528280.1:n.385C>G
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|
|
NM_001316690.1:c.2192C>G
|
NP_001303619.1:p.Ala731Gly
|
|
NM_017780.3:c.8339C>G
|
NP_060250.2:p.Ala2780Gly
|
|
XM_011517553.1:c.8429C>G
|
XP_011515855.1:p.Ala2810Gly
|
|
XM_011517554.1:c.8429C>G
|
XP_011515856.1:p.Ala2810Gly
|
|
XM_011517555.1:c.8426C>G
|
XP_011515857.1:p.Ala2809Gly
|
|
XM_011517556.1:c.8207C>G
|
XP_011515858.1:p.Ala2736Gly
|
|
XM_011517557.1:c.6416C>G
|
XP_011515859.1:p.Ala2139Gly
|
|
XM_011517558.1:c.5966C>G
|
XP_011515860.1:p.Ala1989Gly
|
|
XM_011517559.1:c.5174C>G
|
XP_011515861.1:p.Ala1725Gly
|
|
XM_011517553.2:c.8429C>G
|
XP_011515855.1:p.Ala2810Gly
|
|
XM_011517554.3:c.8429C>G
|
XP_011515856.1:p.Ala2810Gly
|
|
XM_011517555.2:c.8426C>G
|
XP_011515857.1:p.Ala2809Gly
|
|
XM_017013612.1:c.8429C>G
|
XP_016869101.1:p.Ala2810Gly
|
|
XM_017013613.1:c.8336C>G
|
XP_016869102.1:p.Ala2779Gly
|
|
NM_017780.4:c.8339C>G
MANE Select
|
NP_060250.2:p.Ala2780Gly
|
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