ENST00000247933.9:c.1727A>T
|
ENSP00000247933.4:p.Lys576Met
|
|
ENST00000514224.2:c.1727A>T
MANE Select
|
ENSP00000425081.2:p.Lys576Met
|
|
ENST00000652070.1:n.1783A>T
|
|
|
ENST00000247933.8:c.1727A>T
|
ENSP00000247933.4:p.Lys576Met
|
|
ENST00000514224.1:c.1331A>T
|
ENSP00000425081.1:p.Lys444Met
|
|
ENST00000514417.1:n.119A>T
|
|
|
ENST00000514698.5:n.1834A>T
|
|
|
NM_000203.4:c.1727A>T
|
NP_000194.2:p.Lys576Met
|
|
NR_110313.1:n.1815A>T
|
|
|
XM_006713882.2:c.1331A>T
|
XP_006713945.1:p.Lys444Met
|
|
XM_011513459.1:c.1793A>T
|
XP_011511761.1:p.Lys598Met
|
|
XM_011513460.1:c.1586A>T
|
XP_011511762.1:p.Lys529Met
|
|
XM_011513461.1:c.1520A>T
|
XP_011511763.1:p.Lys507Met
|
|
XM_011513462.1:c.1439A>T
|
XP_011511764.1:p.Lys480Met
|
|
XM_011513463.1:c.1439A>T
|
XP_011511765.1:p.Lys480Met
|
|
XR_924947.1:n.1983A>T
|
|
|
NM_000203.5:c.1727A>T
MANE Select
|
NP_000194.2:p.Lys576Met
|
|
NM_001363576.1:c.1331A>T
|
NP_001350505.1:p.Lys444Met
|
|
XM_011513461.2:c.1520A>T
|
XP_011511763.1:p.Lys507Met
|
|
XM_017008163.1:c.767A>T
|
XP_016863652.1:p.Lys256Met
|
|