ENST00000527168.6:n.426C>G
|
|
|
ENST00000529110.2:c.411C>G
|
ENSP00000435349.2:p.His137Gln
|
|
ENST00000529957.6:n.385C>G
|
|
|
ENST00000683366.1:c.*59C>G
|
ENSP00000507283.1:n.*59C>G
|
|
ENST00000683887.1:c.375C>G
|
ENSP00000506886.1:p.His125Gln
|
|
ENST00000684100.1:n.321C>G
|
|
|
ENST00000684126.1:n.385C>G
|
|
|
ENST00000684688.1:n.952C>G
|
|
|
ENST00000204679.9:c.327C>G
MANE Select
|
ENSP00000204679.4:p.His109Gln
|
|
ENST00000204679.8:c.327C>G
|
ENSP00000204679.4:p.His109Gln
|
|
ENST00000526820.5:c.*229C>G
|
ENSP00000434413.1:n.*229C>G
|
|
ENST00000527076.1:n.1343C>G
|
|
|
ENST00000527168.5:n.363C>G
|
|
|
ENST00000529110.1:c.394C>G
|
|
|
ENST00000529957.5:n.426C>G
|
|
|
NM_032520.4:c.327C>G
|
NP_115909.1:p.His109Gln
|
|
XM_017023782.1:c.375C>G
|
XP_016879271.1:p.His125Gln
|
|
XM_017023783.1:c.-34C>G
|
XP_016879272.1:n.-34C>G
|
|
NM_032520.5:c.327C>G
MANE Select
|
NP_115909.1:p.His109Gln
|
|