ENST00000478003.2:n.2225G>C
|
|
|
ENST00000682276.1:n.1842G>C
|
|
|
ENST00000682892.1:c.1944G>C
|
ENSP00000507214.1:p.Arg648Ser
|
|
ENST00000682952.1:n.2036G>C
|
|
|
ENST00000684455.1:c.1610G>C
|
|
|
ENST00000684642.1:c.1794G>C
|
ENSP00000507355.1:p.Arg598Ser
|
|
ENST00000684740.1:n.2575G>C
|
|
|
ENST00000303236.9:c.2397G>C
MANE Select
|
ENSP00000307235.3:p.Arg799Ser
|
|
ENST00000652099.1:c.2591G>C
|
|
|
ENST00000652736.1:n.2273G>C
|
|
|
ENST00000303236.7:c.2397G>C
|
ENSP00000307235.3:p.Arg799Ser
|
|
ENST00000415570.1:c.2034G>C
|
ENSP00000412076.1:p.Arg678Ser
|
|
ENST00000419748.5:c.1944G>C
|
ENSP00000408325.1:p.Arg648Ser
|
|
ENST00000470706.1:n.49-9G>C
|
|
|
NM_001313915.1:c.1944G>C
|
NP_001300844.1:p.Arg648Ser
|
|
NM_004836.5:c.2397G>C
|
NP_004827.4:p.Arg799Ser
|
|
NM_004836.6:c.2397G>C
|
NP_004827.4:p.Arg799Ser
|
|
NR_110236.1:n.1223C>G
|
|
|
XM_005264649.3:c.1713G>C
|
XP_005264706.1:p.Arg571Ser
|
|
XM_017005376.2:c.1713G>C
|
XP_016860865.1:p.Arg571Ser
|
|
NM_004836.7:c.2397G>C
MANE Select
|
NP_004827.4:p.Arg799Ser
|
|
NM_001313915.2:c.1944G>C
|
NP_001300844.1:p.Arg648Ser
|
|