ENST00000264381.8:c.1625T>G
MANE Select
|
ENSP00000264381.3:p.Leu542Arg
|
|
ENST00000264381.7:c.1625T>G
|
ENSP00000264381.3:p.Leu542Arg
|
|
ENST00000479451.5:c.215T>G
|
ENSP00000418325.1:p.Leu72Arg
|
|
ENST00000482958.1:c.*131T>G
|
ENSP00000419804.1:n.*131T>G
|
|
ENST00000488954.1:c.215T>G
|
ENSP00000418504.1:p.Leu72Arg
|
|
ENST00000497011.5:c.1625T>G
|
ENSP00000419505.1:p.Leu542Arg
|
|
NM_000055.2:c.1625T>G
|
NP_000046.1:p.Leu542Arg
|
|
XM_005247685.1:c.1748T>G
|
XP_005247742.1:p.Leu583Arg
|
|
NM_000055.3:c.1625T>G
|
NP_000046.1:p.Leu542Arg
|
|
NR_137635.1:n.267T>G
|
|
|
NR_137636.1:n.1792T>G
|
|
|
NM_000055.4:c.1625T>G
MANE Select
|
NP_000046.1:p.Leu542Arg
|
|
NR_137635.2:n.218T>G
|
|
|
NR_137636.2:n.1743T>G
|
|
|