ENST00000700559.2:c.1541T>G
|
ENSP00000515065.2:p.Val514Gly
|
|
ENST00000700563.2:c.1541T>G
|
ENSP00000515066.2:p.Val514Gly
|
|
ENST00000700556.1:c.12T>G
|
|
|
ENST00000700559.1:c.756T>G
|
|
|
ENST00000700560.1:n.756T>G
|
|
|
ENST00000700561.1:n.882T>G
|
|
|
ENST00000700563.1:c.1495T>G
|
|
|
ENST00000700564.1:n.1545T>G
|
|
|
ENST00000700565.1:n.1394T>G
|
|
|
ENST00000070846.11:c.1673T>G
|
ENSP00000070846.6:p.Val558Gly
|
|
ENST00000340811.9:c.1541T>G
MANE Select
|
ENSP00000342800.5:p.Val514Gly
|
|
ENST00000070846.10:c.1673T>G
|
ENSP00000070846.6:p.Val558Gly
|
|
ENST00000340811.8:c.1541T>G
|
ENSP00000342800.4:p.Val514Gly
|
|
ENST00000613243.1:c.1673T>G
|
ENSP00000478295.1:p.Val558Gly
|
|
NM_001005242.2:c.1541T>G
|
NP_001005242.2:p.Val514Gly
|
|
NM_004572.3:c.1673T>G , LRG_398t1:c.1673T>G
|
NP_004563.2:p.Val558Gly
|
|
NM_001005242.3:c.1541T>G
MANE Select
|
NP_001005242.2:p.Val514Gly
|
|
NM_004572.4:c.1673T>G
|
NP_004563.2:p.Val558Gly
|
|