ENST00000264381.8:c.1671C>T
MANE Select
|
ENSP00000264381.3:p.Val557=
|
|
ENST00000264381.7:c.1671C>T
|
ENSP00000264381.3:p.Val557=
|
|
ENST00000479451.5:c.261C>T
|
ENSP00000418325.1:p.Val87=
|
|
ENST00000482958.1:c.*177C>T
|
ENSP00000419804.1:n.*177C>T
|
|
ENST00000488954.1:c.261C>T
|
ENSP00000418504.1:p.Val87=
|
|
ENST00000497011.5:c.1671C>T
|
ENSP00000419505.1:p.Val557=
|
|
NM_000055.2:c.1671C>T
|
NP_000046.1:p.Val557=
|
|
XM_005247685.1:c.1794C>T
|
XP_005247742.1:p.Val598=
|
|
NM_000055.3:c.1671C>T
|
NP_000046.1:p.Val557=
|
|
NR_137635.1:n.313C>T
|
|
|
NR_137636.1:n.1838C>T
|
|
|
NM_000055.4:c.1671C>T
MANE Select
|
NP_000046.1:p.Val557=
|
|
NR_137635.2:n.264C>T
|
|
|
NR_137636.2:n.1789C>T
|
|
|