ENST00000478003.2:n.1925A>C
|
|
|
ENST00000682276.1:n.1542A>C
|
|
|
ENST00000682892.1:c.1644A>C
|
ENSP00000507214.1:p.Arg548Ser
|
|
ENST00000682952.1:n.1736A>C
|
|
|
ENST00000684455.1:c.1310A>C
|
|
|
ENST00000684642.1:c.1494A>C
|
ENSP00000507355.1:p.Arg498Ser
|
|
ENST00000684740.1:n.2275A>C
|
|
|
ENST00000303236.9:c.2097A>C
MANE Select
|
ENSP00000307235.3:p.Arg699Ser
|
|
ENST00000652099.1:c.2291A>C
|
|
|
ENST00000652736.1:n.1973A>C
|
|
|
ENST00000303236.7:c.2097A>C
|
ENSP00000307235.3:p.Arg699Ser
|
|
ENST00000415570.1:c.1734A>C
|
ENSP00000412076.1:p.Arg578Ser
|
|
ENST00000419748.5:c.1644A>C
|
ENSP00000408325.1:p.Arg548Ser
|
|
ENST00000470706.1:n.23A>C
|
|
|
ENST00000478003.1:n.663A>C
|
|
|
NM_001313915.1:c.1644A>C
|
NP_001300844.1:p.Arg548Ser
|
|
NM_004836.5:c.2097A>C
|
NP_004827.4:p.Arg699Ser
|
|
NM_004836.6:c.2097A>C
|
NP_004827.4:p.Arg699Ser
|
|
NR_110236.1:n.1523T>G
|
|
|
XM_005264649.3:c.1413A>C
|
XP_005264706.1:p.Arg471Ser
|
|
XR_939749.1:n.2376A>C
|
|
|
XM_017005376.2:c.1413A>C
|
XP_016860865.1:p.Arg471Ser
|
|
NM_004836.7:c.2097A>C
MANE Select
|
NP_004827.4:p.Arg699Ser
|
|
NM_001313915.2:c.1644A>C
|
NP_001300844.1:p.Arg548Ser
|
|