ENST00000247933.9:c.697C>G
|
ENSP00000247933.4:p.Leu233Val
|
|
ENST00000514224.2:c.697C>G
MANE Select
|
ENSP00000425081.2:p.Leu233Val
|
|
ENST00000652070.1:n.753C>G
|
|
|
ENST00000247933.8:c.697C>G
|
ENSP00000247933.4:p.Leu233Val
|
|
ENST00000502910.5:c.556C>G
|
ENSP00000422952.1:p.Leu186Val
|
|
ENST00000509948.5:c.490C>G
|
ENSP00000424227.1:p.Leu164Val
|
|
ENST00000514192.5:c.514C>G
|
ENSP00000423685.1:p.Leu172Val
|
|
ENST00000514224.1:c.301C>G
|
ENSP00000425081.1:p.Leu101Val
|
|
ENST00000514698.5:n.597C>G
|
|
|
NM_000203.4:c.697C>G
|
NP_000194.2:p.Leu233Val
|
|
NR_110313.1:n.785C>G
|
|
|
XM_006713882.2:c.301C>G
|
XP_006713945.1:p.Leu101Val
|
|
XM_011513459.1:c.556C>G
|
XP_011511761.1:p.Leu186Val
|
|
XM_011513460.1:c.556C>G
|
XP_011511762.1:p.Leu186Val
|
|
XM_011513461.1:c.490C>G
|
XP_011511763.1:p.Leu164Val
|
|
XM_011513462.1:c.409C>G
|
XP_011511764.1:p.Leu137Val
|
|
XM_011513463.1:c.409C>G
|
XP_011511765.1:p.Leu137Val
|
|
XR_924947.1:n.766C>G
|
|
|
NM_000203.5:c.697C>G
MANE Select
|
NP_000194.2:p.Leu233Val
|
|
NM_001363576.1:c.301C>G
|
NP_001350505.1:p.Leu101Val
|
|
XM_011513461.2:c.490C>G
|
XP_011511763.1:p.Leu164Val
|
|
XM_017008163.1:c.-264C>G
|
XP_016863652.1:n.-264C>G
|
|