ENST00000393564.7:c.1456A>C
|
ENSP00000377194.2:p.Ser486Arg
|
|
ENST00000439227.6:c.1459A>C
|
ENSP00000395599.2:p.Ser487Arg
|
|
ENST00000696420.1:c.1456A>C
|
ENSP00000512615.1:p.Arg486=
|
|
ENST00000696421.1:c.1456A>C
|
ENSP00000512616.1:p.Ser486Arg
|
|
ENST00000696422.1:c.1319A>C
|
|
|
ENST00000696423.1:c.1322A>C
|
|
|
ENST00000696424.1:c.1308A>C
|
ENSP00000512619.1:n.1308A>C
|
|
ENST00000696425.1:c.*369A>C
|
ENSP00000512620.1:n.*369A>C
|
|
ENST00000696426.1:c.*916A>C
|
ENSP00000512621.1:n.*916A>C
|
|
ENST00000696427.1:c.*416A>C
|
ENSP00000512622.1:n.*416A>C
|
|
ENST00000696428.1:c.*1298A>C
|
ENSP00000512623.1:n.*1298A>C
|
|
ENST00000696429.1:c.1456A>C
|
ENSP00000512624.1:p.Ser486Arg
|
|
ENST00000696430.1:c.1456A>C
|
ENSP00000512625.1:p.Ser486Arg
|
|
ENST00000393562.10:c.1456A>C
MANE Select
|
ENSP00000377192.3:p.Ser486Arg
|
|
ENST00000369620.6:c.1594A>C
|
ENSP00000358633.2:p.Ser532Arg
|
|
ENST00000393562.6:c.1546A>C
|
ENSP00000377192.2:p.Ser516Arg
|
|
ENST00000393564.6:c.1456A>C
|
ENSP00000377194.2:p.Ser486Arg
|
|
ENST00000490651.1:n.677A>C
|
|
|
ENST00000621232.4:c.1456A>C
|
ENSP00000483686.1:p.Ser486Arg
|
|
NM_000402.4:c.1546A>C
|
NP_000393.4:p.Ser516Arg
|
|
NM_001042351.2:c.1456A>C
|
NP_001035810.1:p.Ser486Arg
|
|
XM_005274657.2:c.1549A>C
|
XP_005274714.1:p.Ser517Arg
|
|
XM_005274658.2:c.1459A>C
|
XP_005274715.1:p.Ser487Arg
|
|
NM_001360016.2:c.1456A>C
MANE Select
|
NP_001346945.1:p.Ser486Arg
|
|
NM_001042351.3:c.1456A>C
|
NP_001035810.1:p.Ser486Arg
|
|