ENST00000393564.7:c.1069C>G
|
ENSP00000377194.2:p.Arg357Gly
|
|
ENST00000439227.6:c.1072C>G
|
ENSP00000395599.2:p.Arg358Gly
|
|
ENST00000696420.1:c.1069C>G
|
ENSP00000512615.1:p.Arg357Gly
|
|
ENST00000696421.1:c.1069C>G
|
ENSP00000512616.1:p.Arg357Gly
|
|
ENST00000696422.1:c.932C>G
|
|
|
ENST00000696423.1:c.935C>G
|
|
|
ENST00000696424.1:c.921C>G
|
ENSP00000512619.1:n.921C>G
|
|
ENST00000696425.1:c.882C>G
|
ENSP00000512620.1:p.Cys294Trp
|
|
ENST00000696426.1:c.*529C>G
|
ENSP00000512621.1:n.*529C>G
|
|
ENST00000696427.1:c.*29C>G
|
ENSP00000512622.1:n.*29C>G
|
|
ENST00000696428.1:c.*911C>G
|
ENSP00000512623.1:n.*911C>G
|
|
ENST00000696429.1:c.1069C>G
|
ENSP00000512624.1:p.Arg357Gly
|
|
ENST00000696430.1:c.1069C>G
|
ENSP00000512625.1:p.Arg357Gly
|
|
ENST00000393562.10:c.1069C>G
MANE Select
|
ENSP00000377192.3:p.Arg357Gly
|
|
ENST00000369620.6:c.1207C>G
|
ENSP00000358633.2:p.Arg403Gly
|
|
ENST00000393562.6:c.1159C>G
|
ENSP00000377192.2:p.Arg387Gly
|
|
ENST00000393564.6:c.1069C>G
|
ENSP00000377194.2:p.Arg357Gly
|
|
ENST00000490651.1:n.290C>G
|
|
|
ENST00000621232.4:c.1069C>G
|
ENSP00000483686.1:p.Arg357Gly
|
|
NM_000402.4:c.1159C>G
|
NP_000393.4:p.Arg387Gly
|
|
NM_001042351.2:c.1069C>G
|
NP_001035810.1:p.Arg357Gly
|
|
XM_005274657.2:c.1162C>G
|
XP_005274714.1:p.Arg388Gly
|
|
XM_005274658.2:c.1072C>G
|
XP_005274715.1:p.Arg358Gly
|
|
XM_011531132.1:c.975C>G
|
XP_011529434.1:p.Cys325Trp
|
|
NM_001360016.2:c.1069C>G
MANE Select
|
NP_001346945.1:p.Arg357Gly
|
|
NM_001042351.3:c.1069C>G
|
NP_001035810.1:p.Arg357Gly
|
|