ENST00000247933.9:c.873G>T
|
ENSP00000247933.4:p.Ala291=
|
|
ENST00000514224.2:c.873G>T
MANE Select
|
ENSP00000425081.2:p.Ala291=
|
|
ENST00000652070.1:n.929G>T
|
|
|
ENST00000247933.8:c.873G>T
|
ENSP00000247933.4:p.Ala291=
|
|
ENST00000514192.5:c.690G>T
|
ENSP00000423685.1:p.Ala230=
|
|
ENST00000514224.1:c.477G>T
|
ENSP00000425081.1:p.Ala159=
|
|
ENST00000514698.5:n.873G>T
|
|
|
NM_000203.4:c.873G>T
|
NP_000194.2:p.Ala291=
|
|
NR_110313.1:n.961G>T
|
|
|
XM_006713882.2:c.477G>T
|
XP_006713945.1:p.Ala159=
|
|
XM_011513459.1:c.832G>T
|
XP_011511761.1:p.Gly278Ter
|
|
XM_011513460.1:c.732G>T
|
XP_011511762.1:p.Ala244=
|
|
XM_011513461.1:c.666G>T
|
XP_011511763.1:p.Ala222=
|
|
XM_011513462.1:c.585G>T
|
XP_011511764.1:p.Ala195=
|
|
XM_011513463.1:c.585G>T
|
XP_011511765.1:p.Ala195=
|
|
XR_924947.1:n.942G>T
|
|
|
NM_000203.5:c.873G>T
MANE Select
|
NP_000194.2:p.Ala291=
|
|
NM_001363576.1:c.477G>T
|
NP_001350505.1:p.Ala159=
|
|
XM_011513461.2:c.666G>T
|
XP_011511763.1:p.Ala222=
|
|
XM_017008163.1:c.-88G>T
|
XP_016863652.1:n.-88G>T
|
|