ENST00000527168.6:n.913A>G
|
|
|
ENST00000529110.2:c.898A>G
|
ENSP00000435349.2:p.Arg300Gly
|
|
ENST00000529957.6:n.872A>G
|
|
|
ENST00000683366.1:c.*546A>G
|
ENSP00000507283.1:n.*546A>G
|
|
ENST00000683887.1:c.862A>G
|
ENSP00000506886.1:p.Arg288Gly
|
|
ENST00000684100.1:n.808A>G
|
|
|
ENST00000684126.1:n.948A>G
|
|
|
ENST00000684688.1:n.1439A>G
|
|
|
ENST00000204679.9:c.814A>G
MANE Select
|
ENSP00000204679.4:p.Arg272Gly
|
|
ENST00000204679.8:c.814A>G
|
ENSP00000204679.4:p.Arg272Gly
|
|
ENST00000527076.1:n.2037A>G
|
|
|
ENST00000527168.5:n.981A>G
|
|
|
ENST00000529957.5:n.913A>G
|
|
|
NM_032520.4:c.814A>G
|
NP_115909.1:p.Arg272Gly
|
|
XM_017023782.1:c.862A>G
|
XP_016879271.1:p.Arg288Gly
|
|
XM_017023783.1:c.454A>G
|
XP_016879272.1:p.Arg152Gly
|
|
NM_032520.5:c.814A>G
MANE Select
|
NP_115909.1:p.Arg272Gly
|
|