ENST00000350026.11:c.4593G>C
|
ENSP00000055163.8:p.Gln1531His
|
|
ENST00000414678.8:c.4662G>C
|
ENSP00000412835.3:p.Gln1554His
|
|
ENST00000637015.2:c.4881G>C
|
ENSP00000489729.2:p.Gln1627His
|
|
ENST00000346085.10:c.4632G>C
|
ENSP00000344546.5:p.Gln1544His
|
|
ENST00000350026.10:c.4344G>C
|
ENSP00000055163.7:p.Gln1448His
|
|
ENST00000414678.7:c.2910G>C
|
ENSP00000412835.2:p.Gln970His
|
|
ENST00000635849.1:c.2073G>C
|
ENSP00000490948.1:p.Gln691His
|
|
ENST00000635957.1:c.1704G>C
|
ENSP00000490385.1:p.Gln568His
|
|
ENST00000636227.1:n.3215G>C
|
|
|
ENST00000636254.1:n.672G>C
|
|
|
ENST00000636930.2:c.4752G>C
MANE Select
|
ENSP00000490491.2:p.Gln1584His
|
|
ENST00000636940.1:n.2749G>C
|
|
|
ENST00000637015.1:c.2120G>C
|
|
|
ENST00000637568.1:c.2034G>C
|
|
|
ENST00000637741.1:n.1418G>C
|
|
|
ENST00000637810.1:c.2094G>C
|
ENSP00000489636.1:p.Gln698His
|
|
ENST00000637904.1:c.2253G>C
|
ENSP00000490550.1:p.Gln751His
|
|
ENST00000647938.1:c.4383G>C
|
ENSP00000498155.1:p.Gln1461His
|
|
ENST00000346085.9:c.4383G>C
|
ENSP00000344546.4:p.Gln1461His
|
|
ENST00000350026.9:c.4344G>C
|
ENSP00000055163.7:p.Gln1448His
|
|
ENST00000414678.6:c.2910G>C
|
ENSP00000412835.2:p.Gln970His
|
|
NM_017519.2:c.4344G>C
|
NP_059989.2:p.Gln1448His
|
|
NM_020732.3:c.4383G>C
|
NP_065783.3:p.Gln1461His
|
|
XM_005267069.3:c.4503G>C
|
XP_005267126.2:p.Gln1501His
|
|
XM_011535984.1:c.3582G>C
|
XP_011534286.1:p.Gln1194His
|
|
XM_011535985.1:c.3402G>C
|
XP_011534287.1:p.Gln1134His
|
|
XM_011535986.1:c.3162G>C
|
XP_011534288.1:p.Gln1054His
|
|
XM_011535987.1:c.2781G>C
|
XP_011534289.1:p.Gln927His
|
|
XM_011535988.1:c.1644G>C
|
XP_011534290.1:p.Gln548His
|
|
NM_001346813.1:c.4503G>C
|
NP_001333742.1:p.Gln1501His
|
|
NM_001363725.1:c.2253G>C
|
NP_001350654.1:p.Gln751His
|
|
XM_011535984.2:c.4713G>C
|
XP_011534286.2:p.Gln1571His
|
|
XM_011535988.3:c.1644G>C
|
XP_011534290.1:p.Gln548His
|
|
XM_017011103.2:c.4614G>C
|
XP_016866592.1:p.Gln1538His
|
|
XM_017011104.1:c.4584G>C
|
XP_016866593.1:p.Gln1528His
|
|
XM_017011105.2:c.4554G>C
|
XP_016866594.1:p.Gln1518His
|
|
XM_017011106.2:c.4425G>C
|
XP_016866595.1:p.Gln1475His
|
|
XM_017011107.2:c.4404G>C
|
XP_016866596.1:p.Gln1468His
|
|
XR_002956289.1:n.4699G>C
|
|
|
NM_001363725.2:c.2253G>C
|
NP_001350654.1:p.Gln751His
|
|
NM_001371656.1:c.4632G>C
|
NP_001358585.1:p.Gln1544His
|
|
NM_001374820.1:c.4632G>C
|
NP_001361749.1:p.Gln1544His
|
|
NM_001374828.1:c.4752G>C
MANE Select
|
NP_001361757.1:p.Gln1584His
|
|
NM_017519.3:c.4593G>C
|
NP_059989.3:p.Gln1531His
|
|