ENST00000336411.7:c.1407A>C
|
ENSP00000337915.3:p.Gly469=
|
|
ENST00000651162.1:n.749A>C
|
|
|
ENST00000651514.1:c.1314A>C
MANE Select
|
ENSP00000498939.1:p.Gly438=
|
|
ENST00000651783.1:c.855A>C
|
ENSP00000498924.1:p.Gly285=
|
|
ENST00000652018.1:c.1167A>C
|
ENSP00000498733.1:p.Gly389=
|
|
ENST00000336411.6:c.1314A>C
|
ENSP00000337915.2:p.Gly438=
|
|
ENST00000354593.6:c.864A>C
|
ENSP00000346607.2:p.Gly288=
|
|
NM_001202855.2:c.1311A>C
|
NP_001189784.1:p.Gly437=
|
|
NM_017460.5:c.1314A>C
|
NP_059488.2:p.Gly438=
|
|
XM_011515841.1:c.1407A>C
|
XP_011514143.1:p.Gly469=
|
|
XM_011515842.1:c.1404A>C
|
XP_011514144.1:p.Gly468=
|
|
NM_017460.6:c.1314A>C
MANE Select
|
NP_059488.2:p.Gly438=
|
|
NM_001202855.3:c.1311A>C
|
NP_001189784.1:p.Gly437=
|
|