ENST00000247933.9:c.858C>G
|
ENSP00000247933.4:p.Leu286=
|
|
ENST00000514224.2:c.858C>G
MANE Select
|
ENSP00000425081.2:p.Leu286=
|
|
ENST00000652070.1:n.914C>G
|
|
|
ENST00000247933.8:c.858C>G
|
ENSP00000247933.4:p.Leu286=
|
|
ENST00000514192.5:c.675C>G
|
ENSP00000423685.1:p.Leu225=
|
|
ENST00000514224.1:c.462C>G
|
ENSP00000425081.1:p.Leu154=
|
|
ENST00000514698.5:n.858C>G
|
|
|
NM_000203.4:c.858C>G
|
NP_000194.2:p.Leu286=
|
|
NR_110313.1:n.946C>G
|
|
|
XM_006713882.2:c.462C>G
|
XP_006713945.1:p.Leu154=
|
|
XM_011513459.1:c.817C>G
|
XP_011511761.1:p.Leu273Val
|
|
XM_011513460.1:c.717C>G
|
XP_011511762.1:p.Leu239=
|
|
XM_011513461.1:c.651C>G
|
XP_011511763.1:p.Leu217=
|
|
XM_011513462.1:c.570C>G
|
XP_011511764.1:p.Leu190=
|
|
XM_011513463.1:c.570C>G
|
XP_011511765.1:p.Leu190=
|
|
XR_924947.1:n.927C>G
|
|
|
NM_000203.5:c.858C>G
MANE Select
|
NP_000194.2:p.Leu286=
|
|
NM_001363576.1:c.462C>G
|
NP_001350505.1:p.Leu154=
|
|
XM_011513461.2:c.651C>G
|
XP_011511763.1:p.Leu217=
|
|
XM_017008163.1:c.-103C>G
|
XP_016863652.1:n.-103C>G
|
|