ENST00000682568.1:n.1873C>G
|
|
|
ENST00000682617.1:c.1933C>G
|
ENSP00000507912.1:p.Pro645Ala
|
|
ENST00000682826.1:c.*1109C>G
|
ENSP00000507274.1:n.*1109C>G
|
|
ENST00000682909.1:n.3835C>G
|
|
|
ENST00000683277.1:n.3440C>G
|
|
|
ENST00000683407.1:n.1803C>G
|
|
|
ENST00000683962.1:c.*1489C>G
|
ENSP00000506854.1:n.*1489C>G
|
|
ENST00000311895.8:c.1795C>G
MANE Select
|
ENSP00000310520.7:p.Pro599Ala
|
|
ENST00000311895.7:c.1795C>G
|
ENSP00000310520.7:p.Pro599Ala
|
|
ENST00000389138.7:n.1072C>G
|
|
|
NM_005236.2:c.1795C>G , LRG_463t1:c.1795C>G
|
NP_005227.1:p.Pro599Ala
|
|
XM_011522424.1:c.1933C>G
|
XP_011520726.1:p.Pro645Ala
|
|
XM_011522425.1:c.1252C>G
|
XP_011520727.1:p.Pro418Ala
|
|
XM_011522426.1:c.1006C>G
|
XP_011520728.1:p.Pro336Ala
|
|
XM_011522427.1:c.445C>G
|
XP_011520729.1:p.Pro149Ala
|
|
XR_932805.1:n.1954C>G
|
|
|
XM_011522424.3:c.1933C>G
|
XP_011520726.1:p.Pro645Ala
|
|
XM_017023043.2:c.1006C>G
|
XP_016878532.1:p.Pro336Ala
|
|
NM_005236.3:c.1795C>G
MANE Select
|
NP_005227.1:p.Pro599Ala
|
|