ENST00000700555.2:n.270C>G
|
|
|
ENST00000700559.2:c.1758C>G
|
ENSP00000515065.2:p.Ile586Met
|
|
ENST00000700563.2:c.1758C>G
|
ENSP00000515066.2:p.Ile586Met
|
|
ENST00000546498.2:n.445C>G
|
|
|
ENST00000700555.1:c.198C>G
|
ENSP00000515062.1:p.Ile66Met
|
|
ENST00000700556.1:c.229C>G
|
|
|
ENST00000700559.1:c.973C>G
|
|
|
ENST00000700560.1:n.973C>G
|
|
|
ENST00000700561.1:n.1099C>G
|
|
|
ENST00000700563.1:c.1712C>G
|
|
|
ENST00000700564.1:n.1762C>G
|
|
|
ENST00000070846.11:c.1890C>G
|
ENSP00000070846.6:p.Ile630Met
|
|
ENST00000340811.9:c.1758C>G
MANE Select
|
ENSP00000342800.5:p.Ile586Met
|
|
ENST00000070846.10:c.1890C>G
|
ENSP00000070846.6:p.Ile630Met
|
|
ENST00000340811.8:c.1758C>G
|
ENSP00000342800.4:p.Ile586Met
|
|
ENST00000546498.1:n.445C>G
|
|
|
ENST00000552612.5:n.179C>G
|
|
|
ENST00000613243.1:c.1890C>G
|
ENSP00000478295.1:p.Ile630Met
|
|
NM_001005242.2:c.1758C>G
|
NP_001005242.2:p.Ile586Met
|
|
NM_004572.3:c.1890C>G , LRG_398t1:c.1890C>G
|
NP_004563.2:p.Ile630Met
|
|
NM_001005242.3:c.1758C>G
MANE Select
|
NP_001005242.2:p.Ile586Met
|
|
NM_004572.4:c.1890C>G
|
NP_004563.2:p.Ile630Met
|
|