ENST00000264381.8:c.306A>G
MANE Select
|
ENSP00000264381.3:p.Pro102=
|
|
ENST00000264381.7:c.306A>G
|
ENSP00000264381.3:p.Pro102=
|
|
ENST00000479451.5:c.107+6586A>G
|
ENSP00000418325.1:n.107+6586A>G
|
|
ENST00000482958.1:c.306A>G
|
ENSP00000419804.1:p.Pro102=
|
|
ENST00000488954.1:c.107+6586A>G
|
ENSP00000418504.1:n.107+6586A>G
|
|
ENST00000497011.5:c.306A>G
|
ENSP00000419505.1:p.Pro102=
|
|
NM_000055.2:c.306A>G
|
NP_000046.1:p.Pro102=
|
|
XM_005247685.1:c.429A>G
|
XP_005247742.1:p.Pro143=
|
|
NM_000055.3:c.306A>G
|
NP_000046.1:p.Pro102=
|
|
NR_137635.1:n.159+6586A>G
|
|
|
NR_137636.1:n.473A>G
|
|
|
NM_000055.4:c.306A>G
MANE Select
|
NP_000046.1:p.Pro102=
|
|
NR_137635.2:n.110+6586A>G
|
|
|
NR_137636.2:n.424A>G
|
|
|