ENST00000645828.1:n.2726C>T
|
|
|
ENST00000651671.1:c.4919C>T
MANE Select
|
ENSP00000498587.1:p.Ala1640Val
|
|
ENST00000679595.1:c.4919C>T
|
ENSP00000506241.1:p.Ala1640Val
|
|
ENST00000680133.1:c.4805C>T
|
ENSP00000505319.1:p.Ala1602Val
|
|
ENST00000680218.1:c.4799C>T
|
ENSP00000505339.1:p.Ala1600Val
|
|
ENST00000680668.1:c.4805C>T
|
ENSP00000506336.1:p.Ala1602Val
|
|
ENST00000680778.1:c.2516C>T
|
ENSP00000506033.1:p.Ala839Val
|
|
ENST00000680924.1:c.*2319C>T
|
ENSP00000506031.1:n.*2319C>T
|
|
ENST00000681135.1:c.*2528C>T
|
ENSP00000506636.1:n.*2528C>T
|
|
ENST00000681298.1:n.1732C>T
|
|
|
ENST00000681454.1:c.*4155C>T
|
ENSP00000505763.1:n.*4155C>T
|
|
ENST00000277541.6:c.4919C>T
|
ENSP00000277541.6:p.Ala1640Val
|
|
ENST00000494783.1:n.74C>T
|
|
|
NM_017617.3:c.4919C>T
|
NP_060087.3:p.Ala1640Val
|
|
XM_011518717.1:c.4220C>T
|
XP_011517019.1:p.Ala1407Val
|
|
NM_017617.5:c.4919C>T
MANE Select
|
NP_060087.3:p.Ala1640Val
|
|
XM_011518717.2:c.4196C>T
|
XP_011517019.2:p.Ala1399Val
|
|