ENST00000350026.11:c.5009C>A
|
ENSP00000055163.8:p.Pro1670His
|
|
ENST00000414678.8:c.5078C>A
|
ENSP00000412835.3:p.Pro1693His
|
|
ENST00000637015.2:c.5297C>A
|
ENSP00000489729.2:p.Pro1766His
|
|
ENST00000346085.10:c.5048C>A
|
ENSP00000344546.5:p.Pro1683His
|
|
ENST00000350026.10:c.4760C>A
|
ENSP00000055163.7:p.Pro1587His
|
|
ENST00000414678.7:c.3326C>A
|
ENSP00000412835.2:p.Pro1109His
|
|
ENST00000635849.1:c.2489C>A
|
ENSP00000490948.1:p.Pro830His
|
|
ENST00000635957.1:c.2120C>A
|
ENSP00000490385.1:p.Pro707His
|
|
ENST00000636227.1:n.3631C>A
|
|
|
ENST00000636254.1:n.1088C>A
|
|
|
ENST00000636930.2:c.5168C>A
MANE Select
|
ENSP00000490491.2:p.Pro1723His
|
|
ENST00000636940.1:n.3165C>A
|
|
|
ENST00000637015.1:c.2536C>A
|
|
|
ENST00000637568.1:c.2450C>A
|
|
|
ENST00000637741.1:n.1834C>A
|
|
|
ENST00000637810.1:c.2510C>A
|
ENSP00000489636.1:p.Pro837His
|
|
ENST00000637904.1:c.2669C>A
|
ENSP00000490550.1:p.Pro890His
|
|
ENST00000647938.1:c.4799C>A
|
ENSP00000498155.1:p.Pro1600His
|
|
ENST00000346085.9:c.4799C>A
|
ENSP00000344546.4:p.Pro1600His
|
|
ENST00000350026.9:c.4760C>A
|
ENSP00000055163.7:p.Pro1587His
|
|
ENST00000414678.6:c.3326C>A
|
ENSP00000412835.2:p.Pro1109His
|
|
NM_017519.2:c.4760C>A
|
NP_059989.2:p.Pro1587His
|
|
NM_020732.3:c.4799C>A
|
NP_065783.3:p.Pro1600His
|
|
XM_005267069.3:c.4919C>A
|
XP_005267126.2:p.Pro1640His
|
|
XM_011535984.1:c.3998C>A
|
XP_011534286.1:p.Pro1333His
|
|
XM_011535985.1:c.3818C>A
|
XP_011534287.1:p.Pro1273His
|
|
XM_011535986.1:c.3578C>A
|
XP_011534288.1:p.Pro1193His
|
|
XM_011535987.1:c.3197C>A
|
XP_011534289.1:p.Pro1066His
|
|
XM_011535988.1:c.2060C>A
|
XP_011534290.1:p.Pro687His
|
|
NM_001346813.1:c.4919C>A
|
NP_001333742.1:p.Pro1640His
|
|
NM_001363725.1:c.2669C>A
|
NP_001350654.1:p.Pro890His
|
|
XM_011535984.2:c.5129C>A
|
XP_011534286.2:p.Pro1710His
|
|
XM_011535988.3:c.2060C>A
|
XP_011534290.1:p.Pro687His
|
|
XM_017011103.2:c.5030C>A
|
XP_016866592.1:p.Pro1677His
|
|
XM_017011104.1:c.5000C>A
|
XP_016866593.1:p.Pro1667His
|
|
XM_017011105.2:c.4970C>A
|
XP_016866594.1:p.Pro1657His
|
|
XM_017011106.2:c.4841C>A
|
XP_016866595.1:p.Pro1614His
|
|
XM_017011107.2:c.4820C>A
|
XP_016866596.1:p.Pro1607His
|
|
XR_002956289.1:n.5115C>A
|
|
|
NM_001363725.2:c.2669C>A
|
NP_001350654.1:p.Pro890His
|
|
NM_001371656.1:c.5048C>A
|
NP_001358585.1:p.Pro1683His
|
|
NM_001374820.1:c.5048C>A
|
NP_001361749.1:p.Pro1683His
|
|
NM_001374828.1:c.5168C>A
MANE Select
|
NP_001361757.1:p.Pro1723His
|
|
NM_017519.3:c.5009C>A
|
NP_059989.3:p.Pro1670His
|
|