ENST00000247933.9:c.808A>G
|
ENSP00000247933.4:p.Ile270Val
|
|
ENST00000514224.2:c.808A>G
MANE Select
|
ENSP00000425081.2:p.Ile270Val
|
|
ENST00000652070.1:n.864A>G
|
|
|
ENST00000247933.8:c.808A>G
|
ENSP00000247933.4:p.Ile270Val
|
|
ENST00000502910.5:c.667A>G
|
ENSP00000422952.1:p.Ile223Val
|
|
ENST00000514192.5:c.625A>G
|
ENSP00000423685.1:p.Ile209Val
|
|
ENST00000514224.1:c.412A>G
|
ENSP00000425081.1:p.Ile138Val
|
|
ENST00000514698.5:n.808A>G
|
|
|
NM_000203.4:c.808A>G
|
NP_000194.2:p.Ile270Val
|
|
NR_110313.1:n.896A>G
|
|
|
XM_006713882.2:c.412A>G
|
XP_006713945.1:p.Ile138Val
|
|
XM_011513459.1:c.767A>G
|
XP_011511761.1:p.His256Arg
|
|
XM_011513460.1:c.667A>G
|
XP_011511762.1:p.Ile223Val
|
|
XM_011513461.1:c.601A>G
|
XP_011511763.1:p.Ile201Val
|
|
XM_011513462.1:c.520A>G
|
XP_011511764.1:p.Ile174Val
|
|
XM_011513463.1:c.520A>G
|
XP_011511765.1:p.Ile174Val
|
|
XR_924947.1:n.877A>G
|
|
|
NM_000203.5:c.808A>G
MANE Select
|
NP_000194.2:p.Ile270Val
|
|
NM_001363576.1:c.412A>G
|
NP_001350505.1:p.Ile138Val
|
|
XM_011513461.2:c.601A>G
|
XP_011511763.1:p.Ile201Val
|
|
XM_017008163.1:c.-153A>G
|
XP_016863652.1:n.-153A>G
|
|