ENST00000264381.8:c.1629T>G
MANE Select
|
ENSP00000264381.3:p.Arg543=
|
|
ENST00000264381.7:c.1629T>G
|
ENSP00000264381.3:p.Arg543=
|
|
ENST00000479451.5:c.219T>G
|
ENSP00000418325.1:p.Arg73=
|
|
ENST00000482958.1:c.*135T>G
|
ENSP00000419804.1:n.*135T>G
|
|
ENST00000488954.1:c.219T>G
|
ENSP00000418504.1:p.Arg73=
|
|
ENST00000497011.5:c.1629T>G
|
ENSP00000419505.1:p.Arg543=
|
|
NM_000055.2:c.1629T>G
|
NP_000046.1:p.Arg543=
|
|
XM_005247685.1:c.1752T>G
|
XP_005247742.1:p.Arg584=
|
|
NM_000055.3:c.1629T>G
|
NP_000046.1:p.Arg543=
|
|
NR_137635.1:n.271T>G
|
|
|
NR_137636.1:n.1796T>G
|
|
|
NM_000055.4:c.1629T>G
MANE Select
|
NP_000046.1:p.Arg543=
|
|
NR_137635.2:n.222T>G
|
|
|
NR_137636.2:n.1747T>G
|
|
|