ENST00000478003.2:n.2035G>A
|
|
|
ENST00000682276.1:n.1652G>A
|
|
|
ENST00000682892.1:c.1754G>A
|
ENSP00000507214.1:p.Ser585Asn
|
|
ENST00000682952.1:n.1846G>A
|
|
|
ENST00000684455.1:c.1420G>A
|
|
|
ENST00000684642.1:c.1604G>A
|
ENSP00000507355.1:p.Ser535Asn
|
|
ENST00000684740.1:n.2385G>A
|
|
|
ENST00000303236.9:c.2207G>A
MANE Select
|
ENSP00000307235.3:p.Ser736Asn
|
|
ENST00000652099.1:c.2401G>A
|
|
|
ENST00000652736.1:n.2083G>A
|
|
|
ENST00000303236.7:c.2207G>A
|
ENSP00000307235.3:p.Ser736Asn
|
|
ENST00000415570.1:c.1844G>A
|
ENSP00000412076.1:p.Ser615Asn
|
|
ENST00000419748.5:c.1754G>A
|
ENSP00000408325.1:p.Ser585Asn
|
|
ENST00000470706.1:n.48+85G>A
|
|
|
NM_001313915.1:c.1754G>A
|
NP_001300844.1:p.Ser585Asn
|
|
NM_004836.5:c.2207G>A
|
NP_004827.4:p.Ser736Asn
|
|
NM_004836.6:c.2207G>A
|
NP_004827.4:p.Ser736Asn
|
|
NR_110236.1:n.1413C>T
|
|
|
XM_005264649.3:c.1523G>A
|
XP_005264706.1:p.Ser508Asn
|
|
XR_939749.1:n.2486G>A
|
|
|
XM_017005376.2:c.1523G>A
|
XP_016860865.1:p.Ser508Asn
|
|
NM_004836.7:c.2207G>A
MANE Select
|
NP_004827.4:p.Ser736Asn
|
|
NM_001313915.2:c.1754G>A
|
NP_001300844.1:p.Ser585Asn
|
|