ENST00000350026.11:c.4652C>A
|
ENSP00000055163.8:p.Pro1551His
|
|
ENST00000414678.8:c.4721C>A
|
ENSP00000412835.3:p.Pro1574His
|
|
ENST00000637015.2:c.4940C>A
|
ENSP00000489729.2:p.Pro1647His
|
|
ENST00000346085.10:c.4691C>A
|
ENSP00000344546.5:p.Pro1564His
|
|
ENST00000350026.10:c.4403C>A
|
ENSP00000055163.7:p.Pro1468His
|
|
ENST00000414678.7:c.2969C>A
|
ENSP00000412835.2:p.Pro990His
|
|
ENST00000635849.1:c.2132C>A
|
ENSP00000490948.1:p.Pro711His
|
|
ENST00000635957.1:c.1763C>A
|
ENSP00000490385.1:p.Pro588His
|
|
ENST00000636227.1:n.3274C>A
|
|
|
ENST00000636254.1:n.731C>A
|
|
|
ENST00000636930.2:c.4811C>A
MANE Select
|
ENSP00000490491.2:p.Pro1604His
|
|
ENST00000636940.1:n.2808C>A
|
|
|
ENST00000637015.1:c.2179C>A
|
|
|
ENST00000637568.1:c.2093C>A
|
|
|
ENST00000637741.1:n.1477C>A
|
|
|
ENST00000637810.1:c.2153C>A
|
ENSP00000489636.1:p.Pro718His
|
|
ENST00000637904.1:c.2312C>A
|
ENSP00000490550.1:p.Pro771His
|
|
ENST00000647938.1:c.4442C>A
|
ENSP00000498155.1:p.Pro1481His
|
|
ENST00000346085.9:c.4442C>A
|
ENSP00000344546.4:p.Pro1481His
|
|
ENST00000350026.9:c.4403C>A
|
ENSP00000055163.7:p.Pro1468His
|
|
ENST00000414678.6:c.2969C>A
|
ENSP00000412835.2:p.Pro990His
|
|
NM_017519.2:c.4403C>A
|
NP_059989.2:p.Pro1468His
|
|
NM_020732.3:c.4442C>A
|
NP_065783.3:p.Pro1481His
|
|
XM_005267069.3:c.4562C>A
|
XP_005267126.2:p.Pro1521His
|
|
XM_011535984.1:c.3641C>A
|
XP_011534286.1:p.Pro1214His
|
|
XM_011535985.1:c.3461C>A
|
XP_011534287.1:p.Pro1154His
|
|
XM_011535986.1:c.3221C>A
|
XP_011534288.1:p.Pro1074His
|
|
XM_011535987.1:c.2840C>A
|
XP_011534289.1:p.Pro947His
|
|
XM_011535988.1:c.1703C>A
|
XP_011534290.1:p.Pro568His
|
|
NM_001346813.1:c.4562C>A
|
NP_001333742.1:p.Pro1521His
|
|
NM_001363725.1:c.2312C>A
|
NP_001350654.1:p.Pro771His
|
|
XM_011535984.2:c.4772C>A
|
XP_011534286.2:p.Pro1591His
|
|
XM_011535988.3:c.1703C>A
|
XP_011534290.1:p.Pro568His
|
|
XM_017011103.2:c.4673C>A
|
XP_016866592.1:p.Pro1558His
|
|
XM_017011104.1:c.4643C>A
|
XP_016866593.1:p.Pro1548His
|
|
XM_017011105.2:c.4613C>A
|
XP_016866594.1:p.Pro1538His
|
|
XM_017011106.2:c.4484C>A
|
XP_016866595.1:p.Pro1495His
|
|
XM_017011107.2:c.4463C>A
|
XP_016866596.1:p.Pro1488His
|
|
XR_002956289.1:n.4758C>A
|
|
|
NM_001363725.2:c.2312C>A
|
NP_001350654.1:p.Pro771His
|
|
NM_001371656.1:c.4691C>A
|
NP_001358585.1:p.Pro1564His
|
|
NM_001374820.1:c.4691C>A
|
NP_001361749.1:p.Pro1564His
|
|
NM_001374828.1:c.4811C>A
MANE Select
|
NP_001361757.1:p.Pro1604His
|
|
NM_017519.3:c.4652C>A
|
NP_059989.3:p.Pro1551His
|
|