ENST00000645828.1:n.2499T>G
|
|
|
ENST00000651671.1:c.4692T>G
MANE Select
|
ENSP00000498587.1:p.His1564Gln
|
|
ENST00000679595.1:c.4692T>G
|
ENSP00000506241.1:p.His1564Gln
|
|
ENST00000680133.1:c.4578T>G
|
ENSP00000505319.1:p.His1526Gln
|
|
ENST00000680218.1:c.4572T>G
|
ENSP00000505339.1:p.His1524Gln
|
|
ENST00000680668.1:c.4578T>G
|
ENSP00000506336.1:p.His1526Gln
|
|
ENST00000680778.1:c.2289T>G
|
ENSP00000506033.1:p.His763Gln
|
|
ENST00000680924.1:c.*2092T>G
|
ENSP00000506031.1:n.*2092T>G
|
|
ENST00000681135.1:c.*2301T>G
|
ENSP00000506636.1:n.*2301T>G
|
|
ENST00000681298.1:n.1505T>G
|
|
|
ENST00000681454.1:c.*3928T>G
|
ENSP00000505763.1:n.*3928T>G
|
|
ENST00000277541.6:c.4692T>G
|
ENSP00000277541.6:p.His1564Gln
|
|
NM_017617.3:c.4692T>G
|
NP_060087.3:p.His1564Gln
|
|
XM_011518717.1:c.3993T>G
|
XP_011517019.1:p.His1331Gln
|
|
NM_017617.5:c.4692T>G
MANE Select
|
NP_060087.3:p.His1564Gln
|
|
XM_011518717.2:c.3969T>G
|
XP_011517019.2:p.His1323Gln
|
|