ENST00000645828.1:n.2748G>T
|
|
|
ENST00000651671.1:c.4941G>T
MANE Select
|
ENSP00000498587.1:p.Gln1647His
|
|
ENST00000679595.1:c.4941G>T
|
ENSP00000506241.1:p.Gln1647His
|
|
ENST00000680133.1:c.4827G>T
|
ENSP00000505319.1:p.Gln1609His
|
|
ENST00000680218.1:c.4821G>T
|
ENSP00000505339.1:p.Gln1607His
|
|
ENST00000680668.1:c.4827G>T
|
ENSP00000506336.1:p.Gln1609His
|
|
ENST00000680778.1:c.2538G>T
|
ENSP00000506033.1:p.Gln846His
|
|
ENST00000680924.1:c.*2341G>T
|
ENSP00000506031.1:n.*2341G>T
|
|
ENST00000681135.1:c.*2550G>T
|
ENSP00000506636.1:n.*2550G>T
|
|
ENST00000681298.1:n.1754G>T
|
|
|
ENST00000681454.1:c.*4177G>T
|
ENSP00000505763.1:n.*4177G>T
|
|
ENST00000277541.6:c.4941G>T
|
ENSP00000277541.6:p.Gln1647His
|
|
ENST00000494783.1:n.96G>T
|
|
|
NM_017617.3:c.4941G>T
|
NP_060087.3:p.Gln1647His
|
|
XM_011518717.1:c.4242G>T
|
XP_011517019.1:p.Gln1414His
|
|
NM_017617.5:c.4941G>T
MANE Select
|
NP_060087.3:p.Gln1647His
|
|
XM_011518717.2:c.4218G>T
|
XP_011517019.2:p.Gln1406His
|
|