ENST00000326003.7:c.292C>A
MANE Select
|
ENSP00000314151.1:p.His98Asn
|
|
ENST00000326003.6:c.292C>A
|
ENSP00000314151.1:p.His98Asn
|
|
ENST00000360617.7:c.292C>A
|
ENSP00000353829.2:p.His98Asn
|
|
ENST00000422986.6:c.264+28C>A
|
ENSP00000393628.2:n.264+28C>A
|
|
ENST00000593997.5:c.292C>A
|
ENSP00000472907.1:p.His98Asn
|
|
ENST00000595392.5:c.292C>A
|
ENSP00000468912.1:p.His98Asn
|
|
ENST00000595952.5:c.207-44C>A
|
ENSP00000471155.1:n.207-44C>A
|
|
ENST00000596185.5:c.*400C>A
|
ENSP00000471648.1:n.*400C>A
|
|
ENST00000596333.1:n.327C>A
|
|
|
ENST00000597286.5:c.181C>A
|
ENSP00000470523.1:p.His61Asn
|
|
ENST00000597483.5:c.207-44C>A
|
ENSP00000472411.1:n.207-44C>A
|
|
ENST00000598145.1:c.276C>A
|
|
|
ENST00000601349.5:n.1571C>A
|
|
|
ENST00000601503.5:c.235C>A
|
ENSP00000472213.1:p.His79Asn
|
|
ENST00000601812.1:n.724C>A
|
|
|
ENST00000617027.4:c.292C>A
|
ENSP00000483513.1:p.His98Asn
|
|
NM_001030047.1:c.292C>A
|
NP_001025218.1:p.His98Asn
|
|
NM_001030048.1:c.207-44C>A
|
NP_001025219.1:n.207-44C>A
|
|
NM_001648.2:c.292C>A
MANE Select
|
NP_001639.1:p.His98Asn
|
|
XM_011526923.1:c.292C>A
|
XP_011525225.1:p.His98Asn
|
|
XM_011526924.1:c.292C>A
|
XP_011525226.1:p.His98Asn
|
|
XR_935817.1:n.327C>A
|
|
|