ENST00000530449.2:n.118T>A
|
|
|
ENST00000698254.1:c.1022T>A
|
ENSP00000513629.1:p.Leu341His
|
|
ENST00000698255.1:c.1442T>A
|
ENSP00000513630.1:p.Leu481His
|
|
ENST00000698256.1:c.959T>A
|
|
|
ENST00000698257.1:n.911T>A
|
|
|
ENST00000698258.1:n.628T>A
|
|
|
ENST00000698259.1:n.394T>A
|
|
|
ENST00000265686.8:c.1493T>A
MANE Select
|
ENSP00000265686.3:p.Leu498His
|
|
ENST00000265686.7:c.1493T>A
|
ENSP00000265686.3:p.Leu498His
|
|
ENST00000525516.1:n.287T>A
|
|
|
ENST00000525724.5:n.805T>A
|
|
|
ENST00000528981.5:c.645T>A
|
|
|
ENST00000532635.5:c.845T>A
|
ENSP00000434407.1:p.Leu282His
|
|
ENST00000533005.5:n.606T>A
|
|
|
NM_006019.3:c.1493T>A
|
NP_006010.2:p.Leu498His
|
|
NM_006053.3:c.845T>A
|
NP_006044.1:p.Leu282His
|
|
XM_005273709.2:c.1493T>A
|
XP_005273766.1:p.Leu498His
|
|
XM_011544726.1:c.1493T>A
|
XP_011543028.1:p.Leu498His
|
|
XM_011544727.1:c.1493T>A
|
XP_011543029.1:p.Leu498His
|
|
XM_011544728.1:c.1493T>A
|
XP_011543030.1:p.Leu498His
|
|
XR_949754.1:n.1497T>A
|
|
|
NM_001351059.1:c.599T>A
|
NP_001337988.1:p.Leu200His
|
|
XM_024448320.1:c.1586T>A
|
XP_024304088.1:p.Leu529His
|
|
XM_024448321.1:c.1586T>A
|
XP_024304089.1:p.Leu529His
|
|
XM_024448322.1:c.1586T>A
|
XP_024304090.1:p.Leu529His
|
|
XM_024448323.1:c.1586T>A
|
XP_024304091.1:p.Leu529His
|
|
XM_024448324.1:c.1586T>A
|
XP_024304092.1:p.Leu529His
|
|
XR_001747721.2:n.1617T>A
|
|
|
XR_001747722.1:n.1630T>A
|
|
|
XR_001747723.2:n.1630T>A
|
|
|
XR_002957115.1:n.1708T>A
|
|
|
NM_006019.4:c.1493T>A
MANE Select
|
NP_006010.2:p.Leu498His
|
|
NM_001351059.2:c.599T>A
|
NP_001337988.1:p.Leu200His
|
|
NM_006053.4:c.845T>A
|
NP_006044.1:p.Leu282His
|
|