ENST00000651671.1:c.6104C>T
MANE Select
|
ENSP00000498587.1:p.Ala2035Val
|
|
ENST00000679595.1:c.*1144C>T
|
ENSP00000506241.1:n.*1144C>T
|
|
ENST00000679969.1:n.2700C>T
|
|
|
ENST00000680003.1:n.2436C>T
|
|
|
ENST00000680133.1:c.5990C>T
|
ENSP00000505319.1:p.Ala1997Val
|
|
ENST00000680218.1:c.5984C>T
|
ENSP00000505339.1:p.Ala1995Val
|
|
ENST00000680668.1:c.5990C>T
|
ENSP00000506336.1:p.Ala1997Val
|
|
ENST00000680778.1:c.3701C>T
|
ENSP00000506033.1:p.Ala1234Val
|
|
ENST00000680924.1:c.*3504C>T
|
ENSP00000506031.1:n.*3504C>T
|
|
ENST00000681135.1:c.*3713C>T
|
ENSP00000506636.1:n.*3713C>T
|
|
ENST00000681298.1:n.4209C>T
|
|
|
ENST00000681454.1:c.*5340C>T
|
ENSP00000505763.1:n.*5340C>T
|
|
ENST00000277541.6:c.6104C>T
|
ENSP00000277541.6:p.Ala2035Val
|
|
NM_017617.3:c.6104C>T
|
NP_060087.3:p.Ala2035Val
|
|
XM_011518717.1:c.5405C>T
|
XP_011517019.1:p.Ala1802Val
|
|
NM_017617.5:c.6104C>T
MANE Select
|
NP_060087.3:p.Ala2035Val
|
|
XM_011518717.2:c.5381C>T
|
XP_011517019.2:p.Ala1794Val
|
|