ENST00000348974.5:c.1767A>T
|
ENSP00000330021.7:p.Pro589=
|
|
ENST00000394236.9:c.1767A>T
MANE Select
|
ENSP00000377783.3:p.Pro589=
|
|
ENST00000407433.6:c.1722A>T
|
ENSP00000385794.2:p.Pro574=
|
|
ENST00000647936.1:c.1644+2094A>T
|
ENSP00000496822.1:n.1644+2094A>T
|
|
ENST00000648381.1:n.1935A>T
|
|
|
ENST00000648853.1:c.1725A>T
|
ENSP00000497262.1:p.Pro575=
|
|
ENST00000649103.1:c.1866A>T
|
ENSP00000497962.1:n.1866A>T
|
|
ENST00000649585.1:c.710A>T
|
ENSP00000498163.1:n.710A>T
|
|
ENST00000650591.1:c.1863A>T
|
ENSP00000497376.1:p.Pro621=
|
|
ENST00000394236.7:c.1767A>T
|
ENSP00000377783.3:p.Pro589=
|
|
ENST00000407433.5:c.1374A>T
|
ENSP00000385794.1:p.Pro458=
|
|
NM_000313.3:c.1767A>T , LRG_572t1:c.1767A>T
|
NP_000304.2:p.Pro589=
|
|
NM_001314077.1:c.1863A>T , LRG_572t2:c.1863A>T
|
NP_001301006.1:p.Pro621=
|
|
NM_000313.4:c.1767A>T
MANE Select
|
NP_000304.2:p.Pro589=
|
|
NM_001314077.2:c.1863A>T
|
NP_001301006.1:p.Pro621=
|
|