ENST00000527168.6:n.835A>T
|
|
|
ENST00000529110.2:c.820A>T
|
ENSP00000435349.2:p.Arg274Trp
|
|
ENST00000529957.6:n.794A>T
|
|
|
ENST00000683366.1:c.*468A>T
|
ENSP00000507283.1:n.*468A>T
|
|
ENST00000683887.1:c.784A>T
|
ENSP00000506886.1:p.Arg262Trp
|
|
ENST00000684100.1:n.730A>T
|
|
|
ENST00000684126.1:n.870A>T
|
|
|
ENST00000684688.1:n.1361A>T
|
|
|
ENST00000204679.9:c.736A>T
MANE Select
|
ENSP00000204679.4:p.Arg246Trp
|
|
ENST00000204679.8:c.736A>T
|
ENSP00000204679.4:p.Arg246Trp
|
|
ENST00000527076.1:n.1959A>T
|
|
|
ENST00000527168.5:n.903A>T
|
|
|
ENST00000529957.5:n.835A>T
|
|
|
NM_032520.4:c.736A>T
|
NP_115909.1:p.Arg246Trp
|
|
XM_017023782.1:c.784A>T
|
XP_016879271.1:p.Arg262Trp
|
|
XM_017023783.1:c.376A>T
|
XP_016879272.1:p.Arg126Trp
|
|
NM_032520.5:c.736A>T
MANE Select
|
NP_115909.1:p.Arg246Trp
|
|