ENST00000478003.2:n.2245T>G
|
|
|
ENST00000682276.1:n.1862T>G
|
|
|
ENST00000682892.1:c.1964T>G
|
ENSP00000507214.1:p.Ile655Arg
|
|
ENST00000682952.1:n.2056T>G
|
|
|
ENST00000684455.1:c.1630T>G
|
|
|
ENST00000684642.1:c.1814T>G
|
ENSP00000507355.1:p.Ile605Arg
|
|
ENST00000684740.1:n.2595T>G
|
|
|
ENST00000303236.9:c.2417T>G
MANE Select
|
ENSP00000307235.3:p.Ile806Arg
|
|
ENST00000652099.1:c.2611T>G
|
|
|
ENST00000652736.1:n.2293T>G
|
|
|
ENST00000303236.7:c.2417T>G
|
ENSP00000307235.3:p.Ile806Arg
|
|
ENST00000415570.1:c.2054T>G
|
ENSP00000412076.1:p.Ile685Arg
|
|
ENST00000419748.5:c.1964T>G
|
ENSP00000408325.1:p.Ile655Arg
|
|
ENST00000470706.1:n.60T>G
|
|
|
NM_001313915.1:c.1964T>G
|
NP_001300844.1:p.Ile655Arg
|
|
NM_004836.5:c.2417T>G
|
NP_004827.4:p.Ile806Arg
|
|
NM_004836.6:c.2417T>G
|
NP_004827.4:p.Ile806Arg
|
|
NR_110236.1:n.1203A>C
|
|
|
XM_005264649.3:c.1733T>G
|
XP_005264706.1:p.Ile578Arg
|
|
XM_017005376.2:c.1733T>G
|
XP_016860865.1:p.Ile578Arg
|
|
NM_004836.7:c.2417T>G
MANE Select
|
NP_004827.4:p.Ile806Arg
|
|
NM_001313915.2:c.1964T>G
|
NP_001300844.1:p.Ile655Arg
|
|