ENST00000593767.3:c.866T>C
|
ENSP00000470692.3:p.Val289Ala
|
|
ENST00000312865.10:c.866T>C
MANE Select
|
ENSP00000326767.5:p.Val289Ala
|
|
ENST00000538643.5:c.227T>C
|
ENSP00000437496.1:p.Val76Ala
|
|
ENST00000595185.5:c.688+609T>C
|
ENSP00000470027.1:n.688+609T>C
|
|
ENST00000612791.4:c.761+395T>C
|
ENSP00000479851.1:n.761+395T>C
|
|
ENST00000612854.4:c.450+1542T>C
|
ENSP00000482155.1:n.450+1542T>C
|
|
ENST00000617849.4:c.158-182T>C
|
ENSP00000484882.1:n.158-182T>C
|
|
ENST00000618715.4:c.158-181T>C
|
ENSP00000480731.1:n.158-181T>C
|
|
ENST00000620467.4:c.866T>C
|
ENSP00000482659.1:p.Val289Ala
|
|
ENST00000622402.4:c.146-5270T>C
|
ENSP00000478074.1:n.146-5270T>C
|
|
NM_030973.3:c.866T>C , LRG_368t1:c.866T>C
|
NP_112235.2:p.Val289Ala
|
|
XM_011527353.1:c.866T>C
|
XP_011525655.1:p.Val289Ala
|
|
NM_001378355.1:c.866T>C
|
NP_001365284.1:p.Val289Ala
|
|
NM_030973.4:c.866T>C
MANE Select
|
NP_112235.2:p.Val289Ala
|
|