ENST00000527168.6:n.916C>G
|
|
|
ENST00000529110.2:c.901C>G
|
ENSP00000435349.2:p.Pro301Ala
|
|
ENST00000529957.6:n.875C>G
|
|
|
ENST00000683366.1:c.*549C>G
|
ENSP00000507283.1:n.*549C>G
|
|
ENST00000683887.1:c.865C>G
|
ENSP00000506886.1:p.Pro289Ala
|
|
ENST00000684100.1:n.811C>G
|
|
|
ENST00000684126.1:n.951C>G
|
|
|
ENST00000684688.1:n.1442C>G
|
|
|
ENST00000204679.9:c.817C>G
MANE Select
|
ENSP00000204679.4:p.Pro273Ala
|
|
ENST00000204679.8:c.817C>G
|
ENSP00000204679.4:p.Pro273Ala
|
|
ENST00000527076.1:n.2040C>G
|
|
|
ENST00000527168.5:n.984C>G
|
|
|
ENST00000529957.5:n.916C>G
|
|
|
NM_032520.4:c.817C>G
|
NP_115909.1:p.Pro273Ala
|
|
XM_017023782.1:c.865C>G
|
XP_016879271.1:p.Pro289Ala
|
|
XM_017023783.1:c.457C>G
|
XP_016879272.1:p.Pro153Ala
|
|
NM_032520.5:c.817C>G
MANE Select
|
NP_115909.1:p.Pro273Ala
|
|