ENST00000264381.8:c.429T>C
MANE Select
|
ENSP00000264381.3:p.Gly143=
|
|
ENST00000264381.7:c.429T>C
|
ENSP00000264381.3:p.Gly143=
|
|
ENST00000479451.5:c.107+6709T>C
|
ENSP00000418325.1:n.107+6709T>C
|
|
ENST00000482958.1:c.429T>C
|
ENSP00000419804.1:p.Gly143=
|
|
ENST00000488954.1:c.107+6709T>C
|
ENSP00000418504.1:n.107+6709T>C
|
|
ENST00000497011.5:c.429T>C
|
ENSP00000419505.1:p.Gly143=
|
|
NM_000055.2:c.429T>C
|
NP_000046.1:p.Gly143=
|
|
XM_005247685.1:c.552T>C
|
XP_005247742.1:p.Gly184=
|
|
NM_000055.3:c.429T>C
|
NP_000046.1:p.Gly143=
|
|
NR_137635.1:n.159+6709T>C
|
|
|
NR_137636.1:n.596T>C
|
|
|
NM_000055.4:c.429T>C
MANE Select
|
NP_000046.1:p.Gly143=
|
|
NR_137635.2:n.110+6709T>C
|
|
|
NR_137636.2:n.547T>C
|
|
|