ENST00000526008.6:c.*849G>A
|
ENSP00000513006.1:n.*849G>A
|
|
ENST00000696967.1:n.1469G>A
|
|
|
ENST00000696970.1:n.947G>A
|
|
|
ENST00000458235.7:c.2292G>A
MANE Select
|
ENSP00000391676.1:p.Pro764=
|
|
ENST00000458235.5:c.2292G>A
|
ENSP00000391676.1:p.Pro764=
|
|
ENST00000527031.5:n.2278+2098G>A
|
|
|
ENST00000527670.5:c.2292G>A
|
ENSP00000432511.1:p.Pro764=
|
|
ENST00000534444.1:c.2292G>A
|
ENSP00000436421.1:p.Pro764=
|
|
NM_000215.3:c.2292G>A , LRG_77t1:c.2292G>A
|
NP_000206.2:p.Pro764=
|
|
XM_005259896.2:c.2421G>A
|
XP_005259953.1:p.Pro807=
|
|
XM_006722745.2:c.2292G>A
|
XP_006722808.1:p.Pro764=
|
|
XM_011527990.1:c.2421G>A
|
XP_011526292.1:p.Pro807=
|
|
XR_430137.2:n.2431G>A
|
|
|
XM_005259896.3:c.2421G>A
|
XP_005259953.1:p.Pro807=
|
|
NM_000215.4:c.2292G>A
MANE Select
|
NP_000206.2:p.Pro764=
|
|