ENST00000700559.2:c.1534T>C
|
ENSP00000515065.2:p.Tyr512His
|
|
ENST00000700563.2:c.1534T>C
|
ENSP00000515066.2:p.Tyr512His
|
|
ENST00000700556.1:c.5T>C
|
|
|
ENST00000700559.1:c.749T>C
|
|
|
ENST00000700560.1:n.749T>C
|
|
|
ENST00000700561.1:n.875T>C
|
|
|
ENST00000700563.1:c.1488T>C
|
|
|
ENST00000700564.1:n.1538T>C
|
|
|
ENST00000700565.1:n.1387T>C
|
|
|
ENST00000070846.11:c.1666T>C
|
ENSP00000070846.6:p.Tyr556His
|
|
ENST00000340811.9:c.1534T>C
MANE Select
|
ENSP00000342800.5:p.Tyr512His
|
|
ENST00000070846.10:c.1666T>C
|
ENSP00000070846.6:p.Tyr556His
|
|
ENST00000340811.8:c.1534T>C
|
ENSP00000342800.4:p.Tyr512His
|
|
ENST00000613243.1:c.1666T>C
|
ENSP00000478295.1:p.Tyr556His
|
|
NM_001005242.2:c.1534T>C
|
NP_001005242.2:p.Tyr512His
|
|
NM_004572.3:c.1666T>C , LRG_398t1:c.1666T>C
|
NP_004563.2:p.Tyr556His
|
|
NM_001005242.3:c.1534T>C
MANE Select
|
NP_001005242.2:p.Tyr512His
|
|
NM_004572.4:c.1666T>C
|
NP_004563.2:p.Tyr556His
|
|