ENST00000264595.7:c.384A>G
MANE Select
|
ENSP00000264595.2:p.Val128=
|
|
ENST00000264595.6:c.384A>G
|
ENSP00000264595.2:p.Val128=
|
|
ENST00000502310.5:c.39A>G
|
ENSP00000423798.1:p.Val13=
|
|
ENST00000506853.5:n.418A>G
|
|
|
ENST00000510635.1:c.80A>G
|
|
|
ENST00000510955.5:n.315+687A>G
|
|
|
NM_000027.3:c.384A>G
|
NP_000018.2:p.Val128=
|
|
NM_001171988.1:c.384A>G
|
NP_001165459.1:p.Val128=
|
|
NR_033655.1:n.512A>G
|
|
|
XM_006714123.2:c.384A>G
|
XP_006714186.1:p.Val128=
|
|
XR_001741155.2:n.478A>G
|
|
|
NM_000027.4:c.384A>G
MANE Select
|
NP_000018.2:p.Val128=
|
|
NM_001171988.2:c.384A>G
|
NP_001165459.1:p.Val128=
|
|
NR_033655.2:n.446A>G
|
|
|