ENST00000700559.2:c.1531T>G
|
ENSP00000515065.2:p.Phe511Val
|
|
ENST00000700563.2:c.1531T>G
|
ENSP00000515066.2:p.Phe511Val
|
|
ENST00000700556.1:c.2T>G
|
|
|
ENST00000700559.1:c.746T>G
|
|
|
ENST00000700560.1:n.746T>G
|
|
|
ENST00000700561.1:n.872T>G
|
|
|
ENST00000700563.1:c.1485T>G
|
|
|
ENST00000700564.1:n.1535T>G
|
|
|
ENST00000700565.1:n.1384T>G
|
|
|
ENST00000070846.11:c.1663T>G
|
ENSP00000070846.6:p.Phe555Val
|
|
ENST00000340811.9:c.1531T>G
MANE Select
|
ENSP00000342800.5:p.Phe511Val
|
|
ENST00000070846.10:c.1663T>G
|
ENSP00000070846.6:p.Phe555Val
|
|
ENST00000340811.8:c.1531T>G
|
ENSP00000342800.4:p.Phe511Val
|
|
ENST00000613243.1:c.1663T>G
|
ENSP00000478295.1:p.Phe555Val
|
|
NM_001005242.2:c.1531T>G
|
NP_001005242.2:p.Phe511Val
|
|
NM_004572.3:c.1663T>G , LRG_398t1:c.1663T>G
|
NP_004563.2:p.Phe555Val
|
|
NM_001005242.3:c.1531T>G
MANE Select
|
NP_001005242.2:p.Phe511Val
|
|
NM_004572.4:c.1663T>G
|
NP_004563.2:p.Phe555Val
|
|