ENST00000264381.8:c.1690A>G
MANE Select
|
ENSP00000264381.3:p.Ile564Val
|
|
ENST00000264381.7:c.1690A>G
|
ENSP00000264381.3:p.Ile564Val
|
|
ENST00000479451.5:c.280A>G
|
ENSP00000418325.1:p.Ile94Val
|
|
ENST00000482958.1:c.*196A>G
|
ENSP00000419804.1:n.*196A>G
|
|
ENST00000497011.5:c.*80A>G
|
ENSP00000419505.1:n.*80A>G
|
|
NM_000055.2:c.1690A>G
|
NP_000046.1:p.Ile564Val
|
|
XM_005247685.1:c.1813A>G
|
XP_005247742.1:p.Ile605Val
|
|
NM_000055.3:c.1690A>G
|
NP_000046.1:p.Ile564Val
|
|
NR_137635.1:n.332A>G
|
|
|
NR_137636.1:n.1936A>G
|
|
|
NM_000055.4:c.1690A>G
MANE Select
|
NP_000046.1:p.Ile564Val
|
|
NR_137635.2:n.283A>G
|
|
|
NR_137636.2:n.1887A>G
|
|
|