ENST00000527168.6:n.640C>G
|
|
|
ENST00000529110.2:c.625C>G
|
ENSP00000435349.2:p.Pro209Ala
|
|
ENST00000529957.6:n.599C>G
|
|
|
ENST00000683366.1:c.*273C>G
|
ENSP00000507283.1:n.*273C>G
|
|
ENST00000683887.1:c.589C>G
|
ENSP00000506886.1:p.Pro197Ala
|
|
ENST00000684100.1:n.535C>G
|
|
|
ENST00000684126.1:n.599C>G
|
|
|
ENST00000684688.1:n.1166C>G
|
|
|
ENST00000204679.9:c.541C>G
MANE Select
|
ENSP00000204679.4:p.Pro181Ala
|
|
ENST00000204679.8:c.541C>G
|
ENSP00000204679.4:p.Pro181Ala
|
|
ENST00000527076.1:n.1688C>G
|
|
|
ENST00000527168.5:n.708C>G
|
|
|
ENST00000529957.5:n.640C>G
|
|
|
NM_032520.4:c.541C>G
|
NP_115909.1:p.Pro181Ala
|
|
XM_017023782.1:c.589C>G
|
XP_016879271.1:p.Pro197Ala
|
|
XM_017023783.1:c.181C>G
|
XP_016879272.1:p.Pro61Ala
|
|
NM_032520.5:c.541C>G
MANE Select
|
NP_115909.1:p.Pro181Ala
|
|