ENST00000478003.2:n.2176A>G
|
|
|
ENST00000682276.1:n.1793A>G
|
|
|
ENST00000682892.1:c.1895A>G
|
ENSP00000507214.1:p.His632Arg
|
|
ENST00000682952.1:n.1987A>G
|
|
|
ENST00000684455.1:c.1561A>G
|
|
|
ENST00000684642.1:c.1745A>G
|
ENSP00000507355.1:p.His582Arg
|
|
ENST00000684740.1:n.2526A>G
|
|
|
ENST00000303236.9:c.2348A>G
MANE Select
|
ENSP00000307235.3:p.His783Arg
|
|
ENST00000652099.1:c.2542A>G
|
|
|
ENST00000652736.1:n.2224A>G
|
|
|
ENST00000303236.7:c.2348A>G
|
ENSP00000307235.3:p.His783Arg
|
|
ENST00000415570.1:c.1985A>G
|
ENSP00000412076.1:p.His662Arg
|
|
ENST00000419748.5:c.1895A>G
|
ENSP00000408325.1:p.His632Arg
|
|
ENST00000470706.1:n.49-58A>G
|
|
|
NM_001313915.1:c.1895A>G
|
NP_001300844.1:p.His632Arg
|
|
NM_004836.5:c.2348A>G
|
NP_004827.4:p.His783Arg
|
|
NM_004836.6:c.2348A>G
|
NP_004827.4:p.His783Arg
|
|
NR_110236.1:n.1272T>C
|
|
|
XM_005264649.3:c.1664A>G
|
XP_005264706.1:p.His555Arg
|
|
XM_017005376.2:c.1664A>G
|
XP_016860865.1:p.His555Arg
|
|
NM_004836.7:c.2348A>G
MANE Select
|
NP_004827.4:p.His783Arg
|
|
NM_001313915.2:c.1895A>G
|
NP_001300844.1:p.His632Arg
|
|