ENST00000526189.3:c.367+66T>C
|
ENSP00000488104.2:n.367+66T>C
|
|
ENST00000533357.5:c.433T>C
MANE Select
|
ENSP00000432943.1:p.Tyr145His
|
|
ENST00000672287.2:c.-156T>C
|
ENSP00000499818.2:n.-156T>C
|
|
ENST00000672602.2:c.433T>C
|
ENSP00000500814.2:p.Tyr145His
|
|
ENST00000674861.1:n.496T>C
|
|
|
ENST00000463290.5:c.433T>C
|
ENSP00000431538.1:p.Tyr145His
|
|
ENST00000491222.5:c.-156T>C
|
ENSP00000431441.1:n.-156T>C
|
|
ENST00000526189.2:c.111+66T>C
|
|
|
ENST00000533357.4:c.433T>C
|
ENSP00000432943.1:p.Tyr145His
|
|
NM_000530.6:c.433T>C , LRG_256t1:c.433T>C
|
NP_000521.2:p.Tyr145His
|
|
NM_000530.7:c.433T>C
|
NP_000521.2:p.Tyr145His
|
|
NM_001315491.1:c.433T>C
|
NP_001302420.1:p.Tyr145His
|
|
XM_017001321.2:c.463T>C
|
XP_016856810.1:p.Tyr155His
|
|
NM_000530.8:c.433T>C
MANE Select
|
NP_000521.2:p.Tyr145His
|
|
NM_001315491.2:c.433T>C
|
NP_001302420.1:p.Tyr145His
|
|