ENST00000526189.3:c.558G>C
|
ENSP00000488104.2:p.Gly186=
|
|
ENST00000533357.5:c.639G>C
MANE Select
|
ENSP00000432943.1:p.Gly213=
|
|
ENST00000672287.2:c.51G>C
|
ENSP00000499818.2:p.Gly17=
|
|
ENST00000672602.2:c.639G>C
|
ENSP00000500814.2:p.Gly213=
|
|
ENST00000674861.1:n.702G>C
|
|
|
ENST00000463290.5:c.639G>C
|
ENSP00000431538.1:p.Gly213=
|
|
ENST00000476410.1:n.99G>C
|
|
|
ENST00000488271.1:n.77G>C
|
|
|
ENST00000491222.5:c.51G>C
|
ENSP00000431441.1:p.Gly17=
|
|
ENST00000526189.2:c.302G>C
|
|
|
ENST00000533357.4:c.639G>C
|
ENSP00000432943.1:p.Gly213=
|
|
NM_000530.6:c.639G>C , LRG_256t1:c.639G>C
|
NP_000521.2:p.Gly213=
|
|
NM_000530.7:c.639G>C
|
NP_000521.2:p.Gly213=
|
|
NM_001315491.1:c.639G>C
|
NP_001302420.1:p.Gly213=
|
|
XM_017001321.2:c.669G>C
|
XP_016856810.1:p.Gly223=
|
|
NM_000530.8:c.639G>C
MANE Select
|
NP_000521.2:p.Gly213=
|
|
NM_001315491.2:c.639G>C
|
NP_001302420.1:p.Gly213=
|
|