ENST00000527168.6:n.535A>C
|
|
|
ENST00000529110.2:c.520A>C
|
ENSP00000435349.2:p.Asn174His
|
|
ENST00000529957.6:n.494A>C
|
|
|
ENST00000683366.1:c.*168A>C
|
ENSP00000507283.1:n.*168A>C
|
|
ENST00000683887.1:c.484A>C
|
ENSP00000506886.1:p.Asn162His
|
|
ENST00000684100.1:n.430A>C
|
|
|
ENST00000684126.1:n.494A>C
|
|
|
ENST00000684688.1:n.1061A>C
|
|
|
ENST00000204679.9:c.436A>C
MANE Select
|
ENSP00000204679.4:p.Asn146His
|
|
ENST00000204679.8:c.436A>C
|
ENSP00000204679.4:p.Asn146His
|
|
ENST00000527076.1:n.1452A>C
|
|
|
ENST00000527168.5:n.472A>C
|
|
|
ENST00000529110.1:c.503A>C
|
|
|
ENST00000529957.5:n.535A>C
|
|
|
NM_032520.4:c.436A>C
|
NP_115909.1:p.Asn146His
|
|
XM_017023782.1:c.484A>C
|
XP_016879271.1:p.Asn162His
|
|
XM_017023783.1:c.76A>C
|
XP_016879272.1:p.Asn26His
|
|
NM_032520.5:c.436A>C
MANE Select
|
NP_115909.1:p.Asn146His
|
|