ENST00000697149.1:c.1370C>G
|
ENSP00000513138.1:n.1370C>G
|
|
ENST00000697150.1:c.1428C>G
|
ENSP00000513139.1:n.1428C>G
|
|
ENST00000697151.1:c.1361C>G
|
ENSP00000513140.1:n.1361C>G
|
|
ENST00000697164.1:c.1441C>G
|
ENSP00000513153.1:p.Pro481Ala
|
|
ENST00000697165.1:c.1228C>G
|
ENSP00000513154.1:p.Pro410Ala
|
|
ENST00000347310.10:c.1531C>G
MANE Select
|
ENSP00000321345.5:p.Pro511Ala
|
|
ENST00000637002.1:c.922C>G
|
ENSP00000490340.1:p.Pro308Ala
|
|
ENST00000347310.9:c.1531C>G
|
ENSP00000321345.5:p.Pro511Ala
|
|
ENST00000395227.2:c.325C>G
|
ENSP00000378652.2:p.Pro109Ala
|
|
ENST00000425614.3:c.766C>G
|
ENSP00000387640.2:p.Pro256Ala
|
|
ENST00000473881.2:c.*357C>G
|
ENSP00000486667.1:n.*357C>G
|
|
NM_144701.2:c.1531C>G
|
NP_653302.2:p.Pro511Ala
|
|
XM_005270516.2:c.769C>G
|
XP_005270573.1:p.Pro257Ala
|
|
XM_011540789.1:c.1621C>G
|
XP_011539091.1:p.Pro541Ala
|
|
XM_011540790.1:c.1531C>G
|
XP_011539092.1:p.Pro511Ala
|
|
XM_011540791.1:c.1531C>G
|
XP_011539093.1:p.Pro511Ala
|
|
XM_011540790.3:c.1531C>G
|
XP_011539092.1:p.Pro511Ala
|
|
XM_011540791.3:c.1531C>G
|
XP_011539093.1:p.Pro511Ala
|
|
XR_001736993.1:n.1611C>G
|
|
|
NM_144701.3:c.1531C>G
MANE Select
|
NP_653302.2:p.Pro511Ala
|
|