ENST00000675785.2:c.797T>G
|
ENSP00000502019.1:p.Val266Gly
|
|
ENST00000373477.9:c.944T>G
MANE Select
|
ENSP00000362576.4:p.Val315Gly
|
|
ENST00000674629.1:c.*492T>G
|
ENSP00000502470.1:n.*492T>G
|
|
ENST00000674654.1:c.*904T>G
|
ENSP00000501729.1:n.*904T>G
|
|
ENST00000675785.1:c.797T>G
|
ENSP00000502019.1:p.Val266Gly
|
|
ENST00000676297.1:c.*1118T>G
|
ENSP00000501596.1:n.*1118T>G
|
|
ENST00000373477.8:c.944T>G
|
ENSP00000362576.4:p.Val315Gly
|
|
ENST00000478828.1:n.411T>G
|
|
|
ENST00000487404.5:n.1254T>G
|
|
|
ENST00000616261.1:c.944T>G
|
ENSP00000484192.1:p.Val315Gly
|
|
NM_003680.3:c.944T>G , LRG_273t1:c.944T>G
|
NP_003671.1:p.Val315Gly
|
|
XM_011542347.1:c.314T>G
|
XP_011540649.1:p.Val105Gly
|
|
XM_011542348.1:c.314T>G
|
XP_011540650.1:p.Val105Gly
|
|
XM_011542347.2:c.314T>G
|
XP_011540649.1:p.Val105Gly
|
|
XM_017002651.2:c.314T>G
|
XP_016858140.1:p.Val105Gly
|
|
NM_003680.4:c.944T>G
MANE Select
|
NP_003671.1:p.Val315Gly
|
|