ENST00000588860.6:c.998T>G
|
ENSP00000465878.2:p.Val333Gly
|
|
ENST00000589076.6:c.998T>G
|
ENSP00000466934.2:p.Val333Gly
|
|
ENST00000589941.2:c.998T>G
|
ENSP00000465874.2:p.Val333Gly
|
|
ENST00000590061.2:c.998T>G
|
ENSP00000464772.2:p.Val333Gly
|
|
ENST00000593223.2:c.998T>G
|
ENSP00000466118.2:p.Val333Gly
|
|
ENST00000611848.2:c.998T>G
|
ENSP00000478613.2:p.Val333Gly
|
|
ENST00000684953.1:n.2370T>G
|
|
|
ENST00000685090.1:n.1449T>G
|
|
|
ENST00000685232.1:n.1106T>G
|
|
|
ENST00000688307.1:n.249T>G
|
|
|
ENST00000688574.1:n.1106T>G
|
|
|
ENST00000688903.1:n.1212T>G
|
|
|
ENST00000691124.1:n.2480T>G
|
|
|
ENST00000342988.8:c.998T>G
MANE Select
|
ENSP00000341551.3:p.Val333Gly
|
|
ENST00000342988.7:c.998T>G
|
ENSP00000341551.3:p.Val333Gly
|
|
ENST00000398417.6:c.998T>G
|
ENSP00000381452.1:p.Val333Gly
|
|
ENST00000588745.5:c.710T>G
|
ENSP00000464901.1:p.Val237Gly
|
|
ENST00000591126.5:n.2999T>G
|
|
|
ENST00000592186.5:c.955+5549T>G
|
ENSP00000468611.1:n.955+5549T>G
|
|
ENST00000611848.1:c.198T>G
|
|
|
NM_005359.5:c.998T>G , LRG_318t1:c.998T>G
|
NP_005350.1:p.Val333Gly
|
|
NM_005359.6:c.998T>G
MANE Select
|
NP_005350.1:p.Val333Gly
|
|