|
ENST00000607071.6:c.*196T>C
|
ENSP00000475855.1:n.*196T>C
|
|
|
ENST00000642244.1:c.272T>C
|
ENSP00000493554.1:p.Phe91Ser
|
|
|
ENST00000642903.1:c.362T>C
|
ENSP00000493559.1:p.Phe121Ser
|
|
|
ENST00000643093.1:n.412T>C
|
|
|
|
ENST00000644972.1:c.362T>C
|
ENSP00000496451.1:p.Phe121Ser
|
|
|
ENST00000645077.1:c.*196T>C
|
ENSP00000496113.1:n.*196T>C
|
|
|
ENST00000645172.1:c.*189+1958T>C
|
ENSP00000495367.1:n.*189+1958T>C
|
|
|
ENST00000646190.1:n.1593T>C
|
|
|
|
ENST00000646208.1:c.98T>C
|
ENSP00000493723.1:p.Phe33Ser
|
|
|
ENST00000646410.1:c.233T>C
|
ENSP00000494205.1:p.Phe78Ser
|
|
|
ENST00000646562.1:c.*196T>C
|
ENSP00000496087.1:n.*196T>C
|
|
|
ENST00000647468.2:c.362T>C
MANE Select
|
ENSP00000496731.1:p.Phe121Ser
|
|
|
ENST00000648111.1:c.*6T>C
|
ENSP00000497275.1:n.*6T>C
|
|
|
ENST00000367101.5:c.362T>C
|
ENSP00000356068.1:p.Phe121Ser
|
|
|
ENST00000367104.7:c.362T>C
|
ENSP00000356071.3:p.Phe121Ser
|
|
|
ENST00000606965.5:c.362T>C
|
ENSP00000475808.1:p.Phe121Ser
|
|
|
ENST00000607000.1:c.362T>C
|
ENSP00000475788.1:p.Phe121Ser
|
|
|
ENST00000607071.5:c.*196T>C
|
ENSP00000475855.1:n.*196T>C
|
|
|
ENST00000607742.5:c.*196T>C
|
ENSP00000475523.1:n.*196T>C
|
|
|
NM_032861.3:c.362T>C
|
NP_116250.3:p.Phe121Ser
|
|
|
NR_073096.1:n.504T>C
|
|
|
|
XM_006715586.1:c.152T>C
|
XP_006715649.1:p.Phe51Ser
|
|
|
XM_011536196.1:c.341T>C
|
XP_011534498.1:p.Phe114Ser
|
|
|
XM_011536197.1:c.362T>C
|
XP_011534499.1:p.Phe121Ser
|
|
|
XM_011536198.1:c.152T>C
|
XP_011534500.1:p.Phe51Ser
|
|
|
XR_942606.1:n.363T>C
|
|
|
|
XM_006715586.3:c.152T>C
|
XP_006715649.1:p.Phe51Ser
|
|
|
XM_011536196.3:c.341T>C
|
XP_011534498.1:p.Phe114Ser
|
|
|
XM_011536198.3:c.152T>C
|
XP_011534500.1:p.Phe51Ser
|
|
|
XM_024446573.1:c.362T>C
|
XP_024302341.1:p.Phe121Ser
|
|
|
XR_001743697.2:n.443T>C
|
|
|
|
XR_942606.2:n.494T>C
|
|
|
|
NM_032861.4:c.362T>C
MANE Select
|
NP_116250.3:p.Phe121Ser
|
|
|
NR_073096.2:n.486T>C
|
|
|
