ENST00000527168.6:n.906C>T
|
|
|
ENST00000529110.2:c.891C>T
|
ENSP00000435349.2:p.Pro297=
|
|
ENST00000529957.6:n.865C>T
|
|
|
ENST00000683366.1:c.*539C>T
|
ENSP00000507283.1:n.*539C>T
|
|
ENST00000683887.1:c.855C>T
|
ENSP00000506886.1:p.Pro285=
|
|
ENST00000684100.1:n.801C>T
|
|
|
ENST00000684126.1:n.941C>T
|
|
|
ENST00000684688.1:n.1432C>T
|
|
|
ENST00000204679.9:c.807C>T
MANE Select
|
ENSP00000204679.4:p.Pro269=
|
|
ENST00000204679.8:c.807C>T
|
ENSP00000204679.4:p.Pro269=
|
|
ENST00000527076.1:n.2030C>T
|
|
|
ENST00000527168.5:n.974C>T
|
|
|
ENST00000529957.5:n.906C>T
|
|
|
NM_032520.4:c.807C>T
|
NP_115909.1:p.Pro269=
|
|
XM_017023782.1:c.855C>T
|
XP_016879271.1:p.Pro285=
|
|
XM_017023783.1:c.447C>T
|
XP_016879272.1:p.Pro149=
|
|
NM_032520.5:c.807C>T
MANE Select
|
NP_115909.1:p.Pro269=
|
|