ENST00000478003.2:n.2218G>C
|
|
|
ENST00000682276.1:n.1835G>C
|
|
|
ENST00000682892.1:c.1937G>C
|
ENSP00000507214.1:p.Arg646Thr
|
|
ENST00000682952.1:n.2029G>C
|
|
|
ENST00000684455.1:c.1603G>C
|
|
|
ENST00000684642.1:c.1787G>C
|
ENSP00000507355.1:p.Arg596Thr
|
|
ENST00000684740.1:n.2568G>C
|
|
|
ENST00000303236.9:c.2390G>C
MANE Select
|
ENSP00000307235.3:p.Arg797Thr
|
|
ENST00000652099.1:c.2584G>C
|
|
|
ENST00000652736.1:n.2266G>C
|
|
|
ENST00000303236.7:c.2390G>C
|
ENSP00000307235.3:p.Arg797Thr
|
|
ENST00000415570.1:c.2027G>C
|
ENSP00000412076.1:p.Arg676Thr
|
|
ENST00000419748.5:c.1937G>C
|
ENSP00000408325.1:p.Arg646Thr
|
|
ENST00000470706.1:n.49-16G>C
|
|
|
NM_001313915.1:c.1937G>C
|
NP_001300844.1:p.Arg646Thr
|
|
NM_004836.5:c.2390G>C
|
NP_004827.4:p.Arg797Thr
|
|
NM_004836.6:c.2390G>C
|
NP_004827.4:p.Arg797Thr
|
|
NR_110236.1:n.1230C>G
|
|
|
XM_005264649.3:c.1706G>C
|
XP_005264706.1:p.Arg569Thr
|
|
XM_017005376.2:c.1706G>C
|
XP_016860865.1:p.Arg569Thr
|
|
NM_004836.7:c.2390G>C
MANE Select
|
NP_004827.4:p.Arg797Thr
|
|
NM_001313915.2:c.1937G>C
|
NP_001300844.1:p.Arg646Thr
|
|