ENST00000295497.13:c.314T>G
|
ENSP00000295497.7:p.Ile105Ser
|
|
ENST00000444394.7:c.314T>G
|
ENSP00000411911.2:p.Ile105Ser
|
|
ENST00000295497.12:c.314T>G
|
ENSP00000295497.7:p.Ile105Ser
|
|
ENST00000409089.7:c.14T>G
|
ENSP00000386322.3:p.Ile5Ser
|
|
ENST00000409900.9:c.689T>G
MANE Select
|
ENSP00000386741.4:p.Ile230Ser
|
|
ENST00000413882.6:c.143T>G
|
ENSP00000410496.2:p.Ile48Ser
|
|
ENST00000425395.6:c.*136T>G
|
ENSP00000405270.2:n.*136T>G
|
|
ENST00000443238.6:c.167T>G
|
ENSP00000409798.2:p.Ile56Ser
|
|
ENST00000444394.6:c.314T>G
|
ENSP00000411911.2:p.Ile105Ser
|
|
ENST00000444573.2:c.533T>G
|
ENSP00000392603.2:p.Ile178Ser
|
|
ENST00000488080.6:n.332T>G
|
|
|
ENST00000650731.1:c.14T>G
|
ENSP00000499146.1:p.Ile5Ser
|
|
ENST00000650938.1:c.213T>G
|
|
|
ENST00000651246.1:c.281T>G
|
ENSP00000498484.1:p.Ile94Ser
|
|
ENST00000651373.1:c.203T>G
|
ENSP00000499174.1:p.Ile68Ser
|
|
ENST00000651501.1:c.*136T>G
|
ENSP00000498894.1:n.*136T>G
|
|
ENST00000651717.1:c.253-11975T>G
|
ENSP00000499124.1:n.253-11975T>G
|
|
ENST00000652036.1:c.314T>G
|
ENSP00000499139.1:p.Ile105Ser
|
|
ENST00000652154.1:n.587T>G
|
|
|
ENST00000295497.11:c.314T>G
|
ENSP00000295497.7:p.Ile105Ser
|
|
ENST00000409089.6:c.14T>G
|
ENSP00000386322.2:p.Ile5Ser
|
|
ENST00000409156.7:c.611T>G
|
ENSP00000386470.3:p.Ile204Ser
|
|
ENST00000409597.5:c.137T>G
|
ENSP00000386469.1:p.Ile46Ser
|
|
ENST00000409900.7:c.689T>G
|
ENSP00000386741.3:p.Ile230Ser
|
|
ENST00000413882.5:c.143T>G
|
ENSP00000410496.1:p.Ile48Ser
|
|
ENST00000425395.5:c.*240T>G
|
ENSP00000405270.1:n.*240T>G
|
|
ENST00000443238.5:c.167T>G
|
ENSP00000409798.1:p.Ile56Ser
|
|
ENST00000444394.5:c.14T>G
|
ENSP00000411911.1:p.Ile5Ser
|
|
ENST00000444573.1:c.314T>G
|
ENSP00000392603.1:p.Ile105Ser
|
|
ENST00000485882.1:n.148T>G
|
|
|
ENST00000488080.5:n.540T>G
|
|
|
NM_001025201.3:c.611T>G
|
NP_001020372.2:p.Ile204Ser
|
|
NM_001206602.1:c.314T>G
|
NP_001193531.1:p.Ile105Ser
|
|
NM_001822.5:c.689T>G
|
NP_001813.1:p.Ile230Ser
|
|
NR_038133.1:n.555T>G
|
|
|
NM_001025201.4:c.611T>G
|
NP_001020372.2:p.Ile204Ser
|
|
NM_001206602.2:c.314T>G
|
NP_001193531.1:p.Ile105Ser
|
|
NM_001371513.1:c.689T>G
|
NP_001358442.1:p.Ile230Ser
|
|
NM_001371514.1:c.740T>G
|
NP_001358443.1:p.Ile247Ser
|
|
NM_001822.7:c.689T>G
MANE Select
|
NP_001813.1:p.Ile230Ser
|
|
NR_038133.2:n.557T>G
|
|
|