|
ENST00000525083.6:n.270A>G
|
|
|
|
ENST00000532101.6:n.269A>G
|
|
|
|
ENST00000532125.2:c.92A>G
|
ENSP00000434178.2:p.Asp31Gly
|
|
|
ENST00000533839.6:c.85+2152A>G
|
ENSP00000509952.1:n.85+2152A>G
|
|
|
ENST00000534011.6:n.368A>G
|
|
|
|
ENST00000685484.1:c.92A>G
|
ENSP00000510622.1:p.Asp31Gly
|
|
|
ENST00000685601.1:c.92A>G
|
ENSP00000510603.1:p.Asp31Gly
|
|
|
ENST00000685765.1:c.92A>G
|
ENSP00000509991.1:p.Asp31Gly
|
|
|
ENST00000685844.1:c.86-1526A>G
|
ENSP00000509820.1:n.86-1526A>G
|
|
|
ENST00000685857.1:n.270A>G
|
|
|
|
ENST00000686242.1:c.86-1526A>G
|
ENSP00000508950.1:n.86-1526A>G
|
|
|
ENST00000686888.1:c.92A>G
|
ENSP00000509619.1:p.Asp31Gly
|
|
|
ENST00000687699.1:c.216A>G
|
ENSP00000508878.1:p.Gly72=
|
|
|
ENST00000687786.1:n.1425A>G
|
|
|
|
ENST00000688588.1:c.92A>G
|
ENSP00000510802.1:p.Asp31Gly
|
|
|
ENST00000688927.1:n.270A>G
|
|
|
|
ENST00000689283.1:c.210-1526A>G
|
ENSP00000509050.1:n.210-1526A>G
|
|
|
ENST00000689477.1:c.168A>G
|
ENSP00000508945.1:p.Gly56=
|
|
|
ENST00000689765.1:c.86-1526A>G
|
ENSP00000509625.1:n.86-1526A>G
|
|
|
ENST00000690512.1:c.86-1035A>G
|
ENSP00000509793.1:n.86-1035A>G
|
|
|
ENST00000692039.1:c.178A>G
|
ENSP00000508821.1:p.Met60Val
|
|
|
ENST00000692336.1:c.92A>G
|
ENSP00000508540.1:p.Asp31Gly
|
|
|
ENST00000693133.1:n.226-1526A>G
|
|
|
|
ENST00000263578.10:c.92A>G
MANE Select
|
ENSP00000263578.5:p.Asp31Gly
|
|
|
ENST00000263578.9:c.92A>G
|
ENSP00000263578.5:p.Asp31Gly
|
|
|
ENST00000524751.5:n.223-1526A>G
|
|
|
|
ENST00000525083.5:n.122-1526A>G
|
|
|
|
ENST00000525770.5:c.86-1526A>G
|
ENSP00000434739.1:n.86-1526A>G
|
|
|
ENST00000526366.5:n.101-276A>G
|
|
|
|
ENST00000526525.1:n.246-1526A>G
|
|
|
|
ENST00000527004.5:c.92A>G
|
ENSP00000436374.1:p.Asp31Gly
|
|
|
ENST00000529802.1:n.142A>G
|
|
|
|
ENST00000532101.5:n.315A>G
|
|
|
|
ENST00000532125.1:c.50A>G
|
ENSP00000434178.1:p.Asp17Gly
|
|
|
ENST00000533839.5:n.237+2152A>G
|
|
|
|
ENST00000534011.5:n.158-1035A>G
|
|
|
|
ENST00000534315.5:n.499A>G
|
|
|
|
NM_017547.3:c.92A>G
|
NP_060017.1:p.Asp31Gly
|
|
|
NR_037647.1:n.253-1526A>G
|
|
|
|
NR_037648.1:n.278A>G
|
|
|
|
XM_006718880.2:c.-447A>G
|
XP_006718943.1:n.-447A>G
|
|
|
XM_006718881.2:c.-232-1526A>G
|
XP_006718944.1:n.-232-1526A>G
|
|
|
XM_011542895.1:c.-419A>G
|
XP_011541197.1:n.-419A>G
|
|
|
XM_011542896.1:c.-439A>G
|
XP_011541198.1:n.-439A>G
|
|
|
XM_006718881.3:c.-232-1526A>G
|
XP_006718944.1:n.-232-1526A>G
|
|
|
XM_011542895.2:c.-419A>G
|
XP_011541197.1:n.-419A>G
|
|
|
XM_011542896.2:c.-439A>G
|
XP_011541198.1:n.-439A>G
|
|
|
XM_017018000.2:c.92A>G
|
XP_016873489.1:p.Asp31Gly
|
|
|
XM_017018001.1:c.-439A>G
|
XP_016873490.1:n.-439A>G
|
|
|
XM_017018002.1:c.-224-1526A>G
|
XP_016873491.1:n.-224-1526A>G
|
|
|
XM_017018003.2:c.-447A>G
|
XP_016873492.1:n.-447A>G
|
|
|
XM_017018004.1:c.-447A>G
|
XP_016873493.1:n.-447A>G
|
|
|
XM_017018005.1:c.-645A>G
|
XP_016873494.1:n.-645A>G
|
|
|
XM_017018006.2:c.-447A>G
|
XP_016873495.1:n.-447A>G
|
|
|
NM_017547.4:c.92A>G
MANE Select
|
NP_060017.1:p.Asp31Gly
|
|
|
NR_037647.2:n.139-1526A>G
|
|
|
|
NR_037648.2:n.269A>G
|
|
|
