ENST00000700555.2:n.1127T>G
|
|
|
ENST00000700557.2:n.716T>G
|
|
|
ENST00000700559.2:c.2434T>G
|
ENSP00000515065.2:p.Tyr812Asp
|
|
ENST00000546498.2:n.1311T>G
|
|
|
ENST00000549461.2:n.1116T>G
|
|
|
ENST00000700555.1:c.*110T>G
|
ENSP00000515062.1:n.*110T>G
|
|
ENST00000700556.1:c.1095T>G
|
|
|
ENST00000700557.1:c.*110T>G
|
ENSP00000515064.1:n.*110T>G
|
|
ENST00000700558.1:n.838T>G
|
|
|
ENST00000700559.1:c.1649T>G
|
|
|
ENST00000700560.1:n.1990T>G
|
|
|
ENST00000070846.11:c.*110T>G
|
ENSP00000070846.6:n.*110T>G
|
|
ENST00000340811.9:c.*110T>G
MANE Select
|
ENSP00000342800.5:n.*110T>G
|
|
ENST00000070846.10:c.*110T>G
|
ENSP00000070846.6:n.*110T>G
|
|
ENST00000340811.8:c.*110T>G
|
ENSP00000342800.4:n.*110T>G
|
|
ENST00000546769.1:n.411T>G
|
|
|
NM_001005242.2:c.*110T>G
|
NP_001005242.2:n.*110T>G
|
|
NM_004572.3:c.*110T>G , LRG_398t1:c.*110T>G
|
NP_004563.2:n.*110T>G
|
|
NM_001005242.3:c.*110T>G
MANE Select
|
NP_001005242.2:n.*110T>G
|
|
NM_004572.4:c.*110T>G
|
NP_004563.2:n.*110T>G
|
|