ENST00000651671.1:c.6128C>T
MANE Select
|
ENSP00000498587.1:p.Ala2043Val
|
|
ENST00000679595.1:c.*1168C>T
|
ENSP00000506241.1:n.*1168C>T
|
|
ENST00000679969.1:n.2724C>T
|
|
|
ENST00000680003.1:n.2460C>T
|
|
|
ENST00000680133.1:c.6014C>T
|
ENSP00000505319.1:p.Ala2005Val
|
|
ENST00000680218.1:c.6008C>T
|
ENSP00000505339.1:p.Ala2003Val
|
|
ENST00000680668.1:c.6014C>T
|
ENSP00000506336.1:p.Ala2005Val
|
|
ENST00000680778.1:c.3725C>T
|
ENSP00000506033.1:p.Ala1242Val
|
|
ENST00000680924.1:c.*3528C>T
|
ENSP00000506031.1:n.*3528C>T
|
|
ENST00000681135.1:c.*3737C>T
|
ENSP00000506636.1:n.*3737C>T
|
|
ENST00000681298.1:n.4233C>T
|
|
|
ENST00000681454.1:c.*5364C>T
|
ENSP00000505763.1:n.*5364C>T
|
|
ENST00000277541.6:c.6128C>T
|
ENSP00000277541.6:p.Ala2043Val
|
|
NM_017617.3:c.6128C>T
|
NP_060087.3:p.Ala2043Val
|
|
XM_011518717.1:c.5429C>T
|
XP_011517019.1:p.Ala1810Val
|
|
NM_017617.5:c.6128C>T
MANE Select
|
NP_060087.3:p.Ala2043Val
|
|
XM_011518717.2:c.5405C>T
|
XP_011517019.2:p.Ala1802Val
|
|