ENST00000463045.3:c.327C>G
|
ENSP00000481376.2:p.Gly109=
|
|
ENST00000491274.6:c.456C>G
|
ENSP00000480482.2:p.Gly152=
|
|
ENST00000375499.8:c.498C>G
MANE Select
|
ENSP00000364649.3:p.Gly166=
|
|
ENST00000375499.7:c.498C>G
|
ENSP00000364649.3:p.Gly166=
|
|
ENST00000463045.2:c.327C>G
|
ENSP00000481376.1:p.Gly109=
|
|
ENST00000475506.1:n.415C>G
|
|
|
ENST00000485515.5:n.432C>G
|
|
|
ENST00000491274.5:c.456C>G
|
ENSP00000480482.1:p.Gly152=
|
|
NM_003000.2:c.498C>G , LRG_316t1:c.498C>G
|
NP_002991.2:p.Gly166=
|
|
NM_003000.3:c.498C>G
MANE Select
|
NP_002991.2:p.Gly166=
|
|