ENST00000526189.3:c.546G>T
|
ENSP00000488104.2:p.Ala182=
|
|
ENST00000533357.5:c.627G>T
MANE Select
|
ENSP00000432943.1:p.Ala209=
|
|
ENST00000672287.2:c.39G>T
|
ENSP00000499818.2:p.Ala13=
|
|
ENST00000672602.2:c.627G>T
|
ENSP00000500814.2:p.Ala209=
|
|
ENST00000674861.1:n.690G>T
|
|
|
ENST00000463290.5:c.627G>T
|
ENSP00000431538.1:p.Ala209=
|
|
ENST00000476410.1:n.87G>T
|
|
|
ENST00000488271.1:n.65G>T
|
|
|
ENST00000491222.5:c.39G>T
|
ENSP00000431441.1:p.Ala13=
|
|
ENST00000526189.2:c.290G>T
|
|
|
ENST00000533357.4:c.627G>T
|
ENSP00000432943.1:p.Ala209=
|
|
NM_000530.6:c.627G>T , LRG_256t1:c.627G>T
|
NP_000521.2:p.Ala209=
|
|
NM_000530.7:c.627G>T
|
NP_000521.2:p.Ala209=
|
|
NM_001315491.1:c.627G>T
|
NP_001302420.1:p.Ala209=
|
|
XM_017001321.2:c.657G>T
|
XP_016856810.1:p.Ala219=
|
|
NM_000530.8:c.627G>T
MANE Select
|
NP_000521.2:p.Ala209=
|
|
NM_001315491.2:c.627G>T
|
NP_001302420.1:p.Ala209=
|
|