ENST00000642683.1:c.679A>G
|
ENSP00000495376.1:p.Thr227Ala
|
|
ENST00000643672.1:c.676A>G
|
ENSP00000494532.1:p.Thr226Ala
|
|
ENST00000645280.1:c.673A>G
|
ENSP00000496690.1:p.Thr225Ala
|
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ENST00000648579.1:c.*24A>G
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ENSP00000497638.1:n.*24A>G
|
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ENST00000650617.1:c.727A>G
MANE Select
|
ENSP00000497532.1:p.Thr243Ala
|
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ENST00000273158.8:c.727A>G
|
ENSP00000273158.3:p.Thr243Ala
|
|
NM_017875.2:c.727A>G
|
NP_060345.2:p.Thr243Ala
|
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XM_006713214.1:c.715A>G
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XP_006713277.1:p.Thr239Ala
|
|
XM_011533869.1:c.709A>G
|
XP_011532171.1:p.Thr237Ala
|
|
XM_011533870.1:c.676A>G
|
XP_011532172.1:p.Thr226Ala
|
|
XM_011533871.1:c.547A>G
|
XP_011532173.1:p.Thr183Ala
|
|
NM_001354798.1:c.626-1887A>G
|
NP_001341727.1:n.626-1887A>G
|
|
NM_017875.4:c.727A>G
MANE Select
|
NP_060345.2:p.Thr243Ala
|
|
XM_006713214.2:c.715A>G
|
XP_006713277.1:p.Thr239Ala
|
|
XM_011533869.2:c.709A>G
|
XP_011532171.1:p.Thr237Ala
|
|
XM_024453611.1:c.673A>G
|
XP_024309379.1:p.Thr225Ala
|
|
NM_001354798.2:c.626-1887A>G
|
NP_001341727.1:n.626-1887A>G
|
|