ENST00000247933.9:c.817C>G
|
ENSP00000247933.4:p.Leu273Val
|
|
ENST00000514224.2:c.817C>G
MANE Select
|
ENSP00000425081.2:p.Leu273Val
|
|
ENST00000652070.1:n.873C>G
|
|
|
ENST00000247933.8:c.817C>G
|
ENSP00000247933.4:p.Leu273Val
|
|
ENST00000514192.5:c.634C>G
|
ENSP00000423685.1:p.Leu212Val
|
|
ENST00000514224.1:c.421C>G
|
ENSP00000425081.1:p.Leu141Val
|
|
ENST00000514698.5:n.817C>G
|
|
|
NM_000203.4:c.817C>G
|
NP_000194.2:p.Leu273Val
|
|
NR_110313.1:n.905C>G
|
|
|
XM_006713882.2:c.421C>G
|
XP_006713945.1:p.Leu141Val
|
|
XM_011513459.1:c.776C>G
|
XP_011511761.1:p.Pro259Arg
|
|
XM_011513460.1:c.676C>G
|
XP_011511762.1:p.Leu226Val
|
|
XM_011513461.1:c.610C>G
|
XP_011511763.1:p.Leu204Val
|
|
XM_011513462.1:c.529C>G
|
XP_011511764.1:p.Leu177Val
|
|
XM_011513463.1:c.529C>G
|
XP_011511765.1:p.Leu177Val
|
|
XR_924947.1:n.886C>G
|
|
|
NM_000203.5:c.817C>G
MANE Select
|
NP_000194.2:p.Leu273Val
|
|
NM_001363576.1:c.421C>G
|
NP_001350505.1:p.Leu141Val
|
|
XM_011513461.2:c.610C>G
|
XP_011511763.1:p.Leu204Val
|
|
XM_017008163.1:c.-144C>G
|
XP_016863652.1:n.-144C>G
|
|