ENST00000527168.6:n.602T>G
|
|
|
ENST00000529110.2:c.587T>G
|
ENSP00000435349.2:p.Val196Gly
|
|
ENST00000529957.6:n.561T>G
|
|
|
ENST00000683366.1:c.*235T>G
|
ENSP00000507283.1:n.*235T>G
|
|
ENST00000683887.1:c.551T>G
|
ENSP00000506886.1:p.Val184Gly
|
|
ENST00000684100.1:n.497T>G
|
|
|
ENST00000684126.1:n.561T>G
|
|
|
ENST00000684688.1:n.1128T>G
|
|
|
ENST00000204679.9:c.503T>G
MANE Select
|
ENSP00000204679.4:p.Val168Gly
|
|
ENST00000204679.8:c.503T>G
|
ENSP00000204679.4:p.Val168Gly
|
|
ENST00000527076.1:n.1519T>G
|
|
|
ENST00000527168.5:n.539T>G
|
|
|
ENST00000529957.5:n.602T>G
|
|
|
NM_032520.4:c.503T>G
|
NP_115909.1:p.Val168Gly
|
|
XM_017023782.1:c.551T>G
|
XP_016879271.1:p.Val184Gly
|
|
XM_017023783.1:c.143T>G
|
XP_016879272.1:p.Val48Gly
|
|
NM_032520.5:c.503T>G
MANE Select
|
NP_115909.1:p.Val168Gly
|
|