ENST00000478003.2:n.2265T>A
|
|
|
ENST00000682276.1:n.1882T>A
|
|
|
ENST00000682892.1:c.1984T>A
|
ENSP00000507214.1:p.Cys662Ser
|
|
ENST00000682952.1:n.2076T>A
|
|
|
ENST00000684455.1:c.1650T>A
|
|
|
ENST00000684642.1:c.1834T>A
|
ENSP00000507355.1:p.Cys612Ser
|
|
ENST00000684740.1:n.2615T>A
|
|
|
ENST00000303236.9:c.2437T>A
MANE Select
|
ENSP00000307235.3:p.Cys813Ser
|
|
ENST00000652099.1:c.2631T>A
|
|
|
ENST00000652736.1:n.2313T>A
|
|
|
ENST00000303236.7:c.2437T>A
|
ENSP00000307235.3:p.Cys813Ser
|
|
ENST00000415570.1:c.2074T>A
|
ENSP00000412076.1:p.Cys692Ser
|
|
ENST00000419748.5:c.1984T>A
|
ENSP00000408325.1:p.Cys662Ser
|
|
ENST00000470706.1:n.80T>A
|
|
|
NM_001313915.1:c.1984T>A
|
NP_001300844.1:p.Cys662Ser
|
|
NM_004836.5:c.2437T>A
|
NP_004827.4:p.Cys813Ser
|
|
NM_004836.6:c.2437T>A
|
NP_004827.4:p.Cys813Ser
|
|
NR_110236.1:n.1183A>T
|
|
|
XM_005264649.3:c.1753T>A
|
XP_005264706.1:p.Cys585Ser
|
|
XM_017005376.2:c.1753T>A
|
XP_016860865.1:p.Cys585Ser
|
|
NM_004836.7:c.2437T>A
MANE Select
|
NP_004827.4:p.Cys813Ser
|
|
NM_001313915.2:c.1984T>A
|
NP_001300844.1:p.Cys662Ser
|
|