ENST00000350026.11:c.3922G>C
|
ENSP00000055163.8:p.Asp1308His
|
|
ENST00000414678.8:c.3991G>C
|
ENSP00000412835.3:p.Asp1331His
|
|
ENST00000637015.2:c.4210G>C
|
ENSP00000489729.2:p.Asp1404His
|
|
ENST00000346085.10:c.3961G>C
|
ENSP00000344546.5:p.Asp1321His
|
|
ENST00000350026.10:c.3673G>C
|
ENSP00000055163.7:p.Asp1225His
|
|
ENST00000414678.7:c.2239G>C
|
ENSP00000412835.2:p.Asp747His
|
|
ENST00000635849.1:c.1402G>C
|
ENSP00000490948.1:p.Asp468His
|
|
ENST00000635957.1:c.1033G>C
|
ENSP00000490385.1:p.Asp345His
|
|
ENST00000636930.2:c.4081G>C
MANE Select
|
ENSP00000490491.2:p.Asp1361His
|
|
ENST00000636940.1:n.2078G>C
|
|
|
ENST00000637015.1:c.1449G>C
|
|
|
ENST00000637568.1:c.1363G>C
|
|
|
ENST00000637741.1:n.747G>C
|
|
|
ENST00000637810.1:c.1423G>C
|
ENSP00000489636.1:p.Asp475His
|
|
ENST00000637904.1:c.1582G>C
|
ENSP00000490550.1:p.Asp528His
|
|
ENST00000647938.1:c.3712G>C
|
ENSP00000498155.1:p.Asp1238His
|
|
ENST00000346085.9:c.3712G>C
|
ENSP00000344546.4:p.Asp1238His
|
|
ENST00000350026.9:c.3673G>C
|
ENSP00000055163.7:p.Asp1225His
|
|
ENST00000414678.6:c.2239G>C
|
ENSP00000412835.2:p.Asp747His
|
|
NM_017519.2:c.3673G>C
|
NP_059989.2:p.Asp1225His
|
|
NM_020732.3:c.3712G>C
|
NP_065783.3:p.Asp1238His
|
|
XM_005267069.3:c.3832G>C
|
XP_005267126.2:p.Asp1278His
|
|
XM_011535984.1:c.2911G>C
|
XP_011534286.1:p.Asp971His
|
|
XM_011535985.1:c.2731G>C
|
XP_011534287.1:p.Asp911His
|
|
XM_011535986.1:c.2491G>C
|
XP_011534288.1:p.Asp831His
|
|
XM_011535987.1:c.2110G>C
|
XP_011534289.1:p.Asp704His
|
|
XM_011535988.1:c.973G>C
|
XP_011534290.1:p.Asp325His
|
|
NM_001346813.1:c.3832G>C
|
NP_001333742.1:p.Asp1278His
|
|
NM_001363725.1:c.1582G>C
|
NP_001350654.1:p.Asp528His
|
|
XM_011535984.2:c.4042G>C
|
XP_011534286.2:p.Asp1348His
|
|
XM_011535988.3:c.973G>C
|
XP_011534290.1:p.Asp325His
|
|
XM_017011103.2:c.3943G>C
|
XP_016866592.1:p.Asp1315His
|
|
XM_017011104.1:c.3913G>C
|
XP_016866593.1:p.Asp1305His
|
|
XM_017011105.2:c.3883G>C
|
XP_016866594.1:p.Asp1295His
|
|
XM_017011106.2:c.3754G>C
|
XP_016866595.1:p.Asp1252His
|
|
XM_017011107.2:c.3733G>C
|
XP_016866596.1:p.Asp1245His
|
|
XR_002956289.1:n.4125G>C
|
|
|
NM_001363725.2:c.1582G>C
|
NP_001350654.1:p.Asp528His
|
|
NM_001371656.1:c.3961G>C
|
NP_001358585.1:p.Asp1321His
|
|
NM_001374820.1:c.3961G>C
|
NP_001361749.1:p.Asp1321His
|
|
NM_001374828.1:c.4081G>C
MANE Select
|
NP_001361757.1:p.Asp1361His
|
|
NM_017519.3:c.3922G>C
|
NP_059989.3:p.Asp1308His
|
|