ENST00000526189.3:c.534A>G
|
ENSP00000488104.2:p.Pro178=
|
|
ENST00000533357.5:c.615A>G
MANE Select
|
ENSP00000432943.1:p.Pro205=
|
|
ENST00000672287.2:c.27A>G
|
ENSP00000499818.2:p.Pro9=
|
|
ENST00000672602.2:c.615A>G
|
ENSP00000500814.2:p.Pro205=
|
|
ENST00000674861.1:n.678A>G
|
|
|
ENST00000463290.5:c.615A>G
|
ENSP00000431538.1:p.Pro205=
|
|
ENST00000476410.1:n.75A>G
|
|
|
ENST00000488271.1:n.53A>G
|
|
|
ENST00000491222.5:c.27A>G
|
ENSP00000431441.1:p.Pro9=
|
|
ENST00000526189.2:c.278A>G
|
|
|
ENST00000533357.4:c.615A>G
|
ENSP00000432943.1:p.Pro205=
|
|
NM_000530.6:c.615A>G , LRG_256t1:c.615A>G
|
NP_000521.2:p.Pro205=
|
|
NM_000530.7:c.615A>G
|
NP_000521.2:p.Pro205=
|
|
NM_001315491.1:c.615A>G
|
NP_001302420.1:p.Pro205=
|
|
XM_017001321.2:c.645A>G
|
XP_016856810.1:p.Pro215=
|
|
NM_000530.8:c.615A>G
MANE Select
|
NP_000521.2:p.Pro205=
|
|
NM_001315491.2:c.615A>G
|
NP_001302420.1:p.Pro205=
|
|