ENST00000527168.6:n.655C>G
|
|
|
ENST00000529110.2:c.640C>G
|
ENSP00000435349.2:p.Arg214Gly
|
|
ENST00000529957.6:n.614C>G
|
|
|
ENST00000683366.1:c.*288C>G
|
ENSP00000507283.1:n.*288C>G
|
|
ENST00000683887.1:c.604C>G
|
ENSP00000506886.1:p.Arg202Gly
|
|
ENST00000684100.1:n.550C>G
|
|
|
ENST00000684126.1:n.614C>G
|
|
|
ENST00000684688.1:n.1181C>G
|
|
|
ENST00000204679.9:c.556C>G
MANE Select
|
ENSP00000204679.4:p.Arg186Gly
|
|
ENST00000204679.8:c.556C>G
|
ENSP00000204679.4:p.Arg186Gly
|
|
ENST00000527076.1:n.1703C>G
|
|
|
ENST00000527168.5:n.723C>G
|
|
|
ENST00000529957.5:n.655C>G
|
|
|
NM_032520.4:c.556C>G
|
NP_115909.1:p.Arg186Gly
|
|
XM_017023782.1:c.604C>G
|
XP_016879271.1:p.Arg202Gly
|
|
XM_017023783.1:c.196C>G
|
XP_016879272.1:p.Arg66Gly
|
|
NM_032520.5:c.556C>G
MANE Select
|
NP_115909.1:p.Arg186Gly
|
|