ENST00000700555.2:n.1663G>A
|
|
|
ENST00000700557.2:n.1252G>A
|
|
|
ENST00000700559.2:c.*501G>A
|
ENSP00000515065.2:n.*501G>A
|
|
ENST00000549461.2:n.1652G>A
|
|
|
ENST00000700555.1:c.*646G>A
|
ENSP00000515062.1:n.*646G>A
|
|
ENST00000700556.1:c.1631G>A
|
|
|
ENST00000700557.1:c.*646G>A
|
ENSP00000515064.1:n.*646G>A
|
|
ENST00000700558.1:n.1374G>A
|
|
|
ENST00000070846.11:c.*646G>A
|
ENSP00000070846.6:n.*646G>A
|
|
ENST00000340811.9:c.*646G>A
MANE Select
|
ENSP00000342800.5:n.*646G>A
|
|
ENST00000070846.10:c.*646G>A
|
ENSP00000070846.6:n.*646G>A
|
|
ENST00000340811.8:c.*646G>A
|
ENSP00000342800.4:n.*646G>A
|
|
NM_001005242.2:c.*646G>A
|
NP_001005242.2:n.*646G>A
|
|
NM_004572.3:c.*646G>A , LRG_398t1:c.*646G>A
|
NP_004563.2:n.*646G>A
|
|
NM_001005242.3:c.*646G>A
MANE Select
|
NP_001005242.2:n.*646G>A
|
|
NM_004572.4:c.*646G>A
|
NP_004563.2:n.*646G>A
|
|